Canonical Allele Identifier: PA916018096
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295752
ClinVar RCV Id: RCV000303142 RCV000399869 RCV001302602 RCV004021423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Arg3258Gln
CA670336
NM_001291860.2:c.9773G>A