Canonical Allele Identifier: PA645396202
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 284377
ClinVar RCV Id: RCV000278295 RCV000372843 RCV000376732 RCV000725443 RCV000765077 RCV004535319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Ala1883Val
CA671844
NM_005529.7:c.5648C>T