Canonical Allele Identifier: PA916018050
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 284844
ClinVar RCV Id: RCV000280103 RCV000332928 RCV000372364 RCV004535333 RCV004021166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Arg2610Gln
CA671046
NM_001291860.2:c.7829G>A