Canonical Allele Identifier: PA658675411
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Ala1236Glu
CA672546
NM_005529.7:c.3707C>A