Canonical Allele Identifier: PA916018074
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295767
ClinVar RCV Id: RCV000322836 RCV000265382 RCV000731075 RCV002520431 RCV002252089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Ala2968Thr
CA670628
NM_001291860.2:c.8902G>A