Canonical Allele Identifier: PA916018091
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_001278789.1:p.Gln3189His
CA670399
NM_001291860.2:c.9567G>C
CA338913841
NM_001291860.2:c.9567G>T