Allele Registry

Canonical Allele Identifier: PA916018168

Gene: HSPG2 HGNC NCBI

ClinVar RCV:

RCV000278239

RCV000375072

RCV001511116

ClinVar Variation:

295700

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278789.1:p.Ser4332Asn	CA669189 NM_001291860.2:c.12995G>A