Canonical Allele Identifier: PA2828083014
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1021697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350158.1:p.Tyr131His
CA371119542
NM_001363229.2:c.391T>C