Canonical Allele Identifier: PA2580186257
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2431623
ClinVar RCV Id: RCV003142259

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu98Val
CA346739896
NM_001281492.2:c.293A>T