Allele Registry

Canonical Allele Identifier: PA645380090

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000216959

RCV000800743

ClinVar Variation:

230718

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro462Thr	CA10578068 NM_000179.3:c.1384C>A