Canonical Allele Identifier: PA645396313
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295756
ClinVar RCV Id: RCV000274765 RCV000367014 RCV000414737 RCV001348418 RCV004543166 RCV002522108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Gln3188His
CA670399
NM_005529.7:c.9564G>C
CA338913841
NM_005529.7:c.9564G>T