Canonical Allele Identifier: PA916018143
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295711
ClinVar RCV Id: RCV000287593 RCV000347270 RCV000757386 RCV000999873 RCV004537645 RCV002278344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Ala3944Thr
CA669606
NM_001291860.2:c.11830G>A