Canonical Allele Identifier: PA645396179
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Phe1497Ile
CA672259
NM_005529.7:c.4489T>A