Canonical Allele Identifier: PA2826626675
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820460
ClinVar RCV Id: RCV001013945
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly531Ser
CA346750625
NM_001281492.2:c.1591G>A