Canonical Allele Identifier: PA916018177
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295693
ClinVar RCV Id: RCV000299146 RCV000407722 RCV001000608 RCV004021422 RCV002059437 RCV004543163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Ala4383Asp
CA669117
NM_001291860.2:c.13148C>A