Canonical Allele Identifier: PA2826624922
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2008181
ClinVar RCV Id: RCV002833678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val120Asp
CA346740120
NM_001281492.2:c.359T>A