Canonical Allele Identifier: PA916018169
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295699
ClinVar RCV Id: RCV000274764 RCV000318163 RCV001521940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Val4333Ile
CA669186
NM_001291860.2:c.12997G>A