Canonical Allele Identifier: PA2826627514
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1793280
ClinVar RCV Id: RCV002426024
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe728Ser
CA346754743
NM_001281492.2:c.2183T>C