Canonical Allele Identifier: PA2826625711
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769250
ClinVar RCV Id: RCV002380688
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Tyr303Asn
CA346744243
NM_001281492.2:c.907T>A