Canonical Allele Identifier: PA658675544
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Gly4345Arg
CA669145
NM_005529.7:c.13033G>A
CA338908452
NM_005529.7:c.13033G>C