Allele Registry

Canonical Allele Identifier: PA916012152

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

180096

ClinVar RCV:

RCV000160697

RCV000226708

RCV000564770

RCV000663071

RCV001175454

RCV003467253

RCV003998504

ClinVar Variation:

182648

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Asn927Ser	CA013811 NM_001281494.2:c.2780A>G