Canonical Allele Identifier: PA2828082732
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1021697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350157.1:p.Tyr355His
CA371119542
NM_001363228.2:c.1063T>C