Canonical Allele Identifier: PA916018132
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295725
ClinVar RCV Id: RCV000269036 RCV000363706 RCV000765074 RCV000948533 RCV000507550 RCV004537646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Thr3692Ile
CA669942
NM_001291860.2:c.11075C>T