Canonical Allele Identifier: PA2826810681
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295907
ClinVar RCV Id: RCV000266127 RCV001367619 RCV002520448 RCV000365315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Arg257Pro
CA673709
NM_001291860.2:c.770G>C