Canonical Allele Identifier: PA916018016
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295812
ClinVar RCV Id: RCV000290427 RCV000384775 RCV000938965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Val2117Met
CA671591
NM_001291860.2:c.6349G>A