HMCN1 c.13750C>T ;(p.P4584S)

Variant ID: 1-186106797-C-T

NM_031935.2(HMCN1):c.13750C>T;(p.P4584S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing.

Computational And Structural Biotechnology Journal
Shi, Xin X; Zhang, Li L; Bai, Kai K; Xie, Huilin H; Shi, Tieliu T; Zhang, Ruilin R; Fu, Qihua Q; Chen, Sun S; Lu, Yanan Y; Yu, Yu Y; Sun, Kun K
Publication Date: 2020

Variant appearance in text: HMCN1: P4584S
PubMed Link: 32128068
Variant Present in the following documents:
  • Main text
  • main.pdf
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