Canonical Allele Identifier: PA916018041
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 198007
ClinVar RCV Id: RCV000179196 RCV000259625 RCV000370645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Arg2481Trp
CA246472
NM_001291860.2:c.7441C>T