Canonical Allele Identifier: PA658809178
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 499443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Val4340Met
CA669150
NM_005529.7:c.13018G>A