Canonical Allele Identifier: PA916018122
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295732
ClinVar RCV Id: RCV000306473 RCV000347343 RCV002520425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Val3541Ile
CA670068
NM_001291860.2:c.10621G>A