Allele Registry

Canonical Allele Identifier: PA916018079

Gene: HSPG2 HGNC NCBI

ClinVar RCV:

RCV000313160

RCV000370135

RCV001518506

RCV002685905

ClinVar Variation:

295764

1951108

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278789.1:p.Ser2996Gly	CA670594 NM_001291860.2:c.8986A>G CA2580061531 NM_001291860.2:c.8985_8986delinsTG