Canonical Allele Identifier: PA2826627281
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp673Gly
CA010206
NM_001281492.2:c.2018A>G