Canonical Allele Identifier: PA250357
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 209161
ClinVar RCV Id: RCV000191094 RCV000883656 RCV001098138 RCV002277446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Asn786Ser
CA250356
NM_005529.7:c.2357A>G