Canonical Allele Identifier: PA354137
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 219294
ClinVar RCV Id: RCV000206750 RCV000215362 RCV000471873 RCV003454537 RCV003462359 RCV003477675
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1211Pro
CA350757
NM_000179.3:c.3632T>C