Canonical Allele Identifier: PA645396322
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Val3402Met
CA670195
NM_005529.7:c.10204G>A