Canonical Allele Identifier: PA2826625540
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 963892
ClinVar RCV Id: RCV001237996
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala263Pro
CA346742352
NM_001281492.2:c.787G>C