Allele Registry

Canonical Allele Identifier: PA2826628703

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000206750

RCV000215362

RCV000471873

RCV003454537

RCV003462359

RCV003477675

ClinVar Variation:

219294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Leu1081Pro	CA350757 NM_001281492.2:c.3242T>C