Allele Registry

Canonical Allele Identifier: PA645381083

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000219912

RCV000233003

RCV000484834

RCV000657004

RCV000662524

RCV003469017

RCV003997865

ClinVar Variation:

230869

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly624Ser	CA10578081 NM_000179.3:c.1870G>A