Allele Registry

Canonical Allele Identifier: PA2826631313

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000524133

RCV000568729

RCV000662512

RCV001582560

RCV003466941

RCV003997072

ClinVar Variation:

89259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Phe424Tyr	CA009822 NM_001281493.2:c.1271T>A