Canonical Allele Identifier: PA916018035
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 290055
ClinVar RCV Id: RCV000285449 RCV000340372 RCV000711940 RCV000765076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Ser2413Asn
CA671265
NM_001291860.2:c.7238G>A