Allele Registry

Canonical Allele Identifier: PA191189

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000164528

RCV000205577

RCV000662485

RCV001580460

RCV002271437

RCV003462138

ClinVar Variation:

185159

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Met875Thr	CA010617 NM_000179.3:c.2624T>C