Allele Registry

Canonical Allele Identifier: PA645380699

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491403

RCV001204099

ClinVar Variation:

428315

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln572Glu	CA346748599 NM_000179.3:c.1714C>G