Canonical Allele Identifier: PA2828083018
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 422050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350158.1:p.Gly135Trp
CA16618645
NM_001363229.2:c.403G>T