Canonical Allele Identifier: PA2826624951
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760056
ClinVar RCV Id: RCV002396474
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser126Cys
CA346740188
NM_001281492.2:c.376A>T