Canonical Allele Identifier: PA916017890
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295892
ClinVar RCV Id: RCV000347946 RCV000383784 RCV000887329 RCV000591375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.His510Tyr
CA673395
NM_001291860.2:c.1528C>T