COMT c.635A>G ;(p.K212R)

Variant ID: 22-19956078-A-G

NM_000754.3(COMT):c.635A>G;(p.K212R)

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:

Identification of a novel haplotype of the human catechol-O-methyltransferase gene.

Pharmacogenetics And Genomics
Bai, Hyoung-Woo HW; Zhu, Bao Ting BT
Publication Date: 2009-01

Variant appearance in text: COMT: K212R
PubMed Link: 19077667
Variant Present in the following documents:
  • Main text
View BVdb publication page