Allele Registry

Canonical Allele Identifier: PA916017970

Gene: HSPG2 HGNC NCBI

ClinVar RCV:

RCV001800294

ClinVar Variation:

14918

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278789.1:p.Cys1533Tyr	CA124452 NM_001291860.2:c.4598G>A