Canonical Allele Identifier: PA2828082231
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1021697
ClinVar RCV Id: RCV001321499 RCV001835614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350156.1:p.Tyr419His
CA371119542
NM_001363227.2:c.1255T>C