Canonical Allele Identifier: PA2828082926
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 420117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350157.1:p.Tyr563Cys
CA4737042
NM_001363228.2:c.1688A>G