Canonical Allele Identifier: PA645396087
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Arg293His
CA673672
NM_005529.7:c.878G>A