Canonical Allele Identifier: PA645396317
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Arg3257Gln
CA670336
NM_005529.7:c.9770G>A