Canonical Allele Identifier: PA916017970
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 14918
ClinVar RCV Id: RCV001800294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Cys1533Tyr
CA124452
NM_001291860.2:c.4598G>A