Canonical Allele Identifier: PA2826810707
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Arg293His
CA673672
NM_001291860.2:c.878G>A