Allele Registry

Canonical Allele Identifier: PA2826634983

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000122952

RCV000218729

RCV000219239

RCV000411179

RCV000524115

RCV000780476

RCV002398584

RCV003460868

RCV003492534

ClinVar Variation:

135830

1776067

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu231Asp	CA008846 NM_001281494.2:c.693G>C CA346746950 NM_001281494.2:c.693G>T