Canonical Allele Identifier: PA916018111
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Arg3428Gln
CA670179
NM_001291860.2:c.10283G>A