Canonical Allele Identifier: PA2826628617
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89422
ClinVar RCV Id: RCV000166108 RCV000679239 RCV001302789 RCV003230394 RCV003450974 RCV003460687 RCV003997093
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1063Lys
CA013478
NM_001281492.2:c.3187G>A