Canonical Allele Identifier: PA645390388
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_689632.2:p.Gly423Trp
CA16618645
NM_152419.3:c.1267G>T