Allele Registry

Canonical Allele Identifier: PA299509

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160711

RCV000217717

RCV000456306

RCV000781604

RCV000986705

RCV001030488

RCV003467255

RCV003998510

ClinVar Variation:

182656

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg178Cys	CA015802 NM_000179.3:c.532C>T