Allele Registry

Canonical Allele Identifier: PA916017897

Gene: HSPG2 HGNC NCBI

ClinVar RCV:

RCV000260399

RCV000296869

RCV000841771

RCV002008982

ClinVar Variation:

295887

1487980

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278789.1:p.Met639Val	CA673246 NM_001291860.2:c.1915A>G CA2573132182 NM_001291860.2:c.1914_1915delinsTG