Canonical Allele Identifier: PA2828081904
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 363141
ClinVar RCV Id: RCV000316013 RCV002058735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350156.1:p.Ala93Ser
CA4736466
NM_001363227.2:c.277G>T