Allele Registry

Canonical Allele Identifier: PA357804

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000210157

RCV000215593

RCV001044010

ClinVar Variation:

224581

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala737Val	CA357802 NM_000179.3:c.2210C>T