Canonical Allele Identifier: PA916018106
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295745
ClinVar RCV Id: RCV000267507 RCV000322617 RCV000757387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Val3403Met
CA670195
NM_001291860.2:c.10207G>A