Allele Registry

Canonical Allele Identifier: PA645380317

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000223633

RCV000467079

RCV001093674

RCV001354875

RCV004532793

ClinVar Variation:

232251

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.His501Tyr	CA067771 NM_000179.3:c.1501C>T