Canonical Allele Identifier: PA645396353
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Val4332Ile
CA669186
NM_005529.7:c.12994G>A