Canonical Allele Identifier: PA2828082293
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350156.1:p.Met482Lys
CA114867
NM_001363227.2:c.1445T>A