Canonical Allele Identifier: PA2826627283
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455196
ClinVar RCV Id: RCV000527339 RCV002456040
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp673Tyr
CA346753957
NM_001281492.2:c.2017G>T