Allele Registry

Canonical Allele Identifier: PA299487

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160697

RCV000226708

RCV000564770

RCV000663071

RCV001175454

RCV003467253

RCV003998504

ClinVar Variation:

182648

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asn1229Ser	CA013811 NM_000179.3:c.3686A>G