Canonical Allele Identifier: PA916017995
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 284377
ClinVar RCV Id: RCV000278295 RCV000372843 RCV000376732 RCV000725443 RCV000765077 RCV004535319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Ala1884Val
CA671844
NM_001291860.2:c.5651C>T