Canonical Allele Identifier: PA2828082737
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 422050
ClinVar RCV Id: RCV000478090 RCV000626050 RCV001074815 RCV001865466 RCV003330719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350157.1:p.Gly359Trp
CA16618645
NM_001363228.2:c.1075G>T