Canonical Allele Identifier: PA645396121
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.His779Tyr
CA673113
NM_005529.7:c.2335C>T