Canonical Allele Identifier: PA916018022
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 284845
ClinVar RCV Id: RCV000259556 RCV000354393 RCV000387513 RCV004535334 RCV002518950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Ala2182Thr
CA671511
NM_001291860.2:c.6544G>A