Canonical Allele Identifier: PA645396085
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Arg257Pro
CA673709
NM_005529.7:c.770G>C