Allele Registry

Canonical Allele Identifier: PA916010979

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000459919

RCV000481267

RCV000566299

RCV000567789

RCV000663030

RCV000805474

RCV001570489

RCV001721501

ClinVar Variation:

410476

483766

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly39Arg	CA067220 NM_001281492.2:c.115G>A CA067226 NM_001281492.2:c.115G>C