Canonical Allele Identifier: PA916011500
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428424
ClinVar RCV Id: RCV000491737
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu989Lys
CA346758765
NM_001281492.2:c.2965G>A