RB1 c.2664T>C ;(p.S888=)

Variant ID: 13-49051491-T-C

NM_000321.2(RB1):c.2664T>C;(p.S888=)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters.

European Journal Of Human Genetics : Ejhg
Publication Date: 2020-12

Variant appearance in text: RB1: 2664T>C
PubMed Link: 33262486
Variant Present in the following documents:
  • Main text
View BVdb publication page