Canonical Allele Identifier: PA645396108
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.His509Tyr
CA673395
NM_005529.7:c.1525C>T