Canonical Allele Identifier: PA645396335
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_005520.4:p.Thr3691Ile
CA669942
NM_005529.7:c.11072C>T