Canonical Allele Identifier: PA916018043
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295789
ClinVar RCV Id: RCV000309917 RCV000348433 RCV000958428 RCV002278359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Thr2512Ile
CA671143
NM_001291860.2:c.7535C>T