Canonical Allele Identifier: PA645396297
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 284843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Ala2869Pro
CA670729
NM_005529.7:c.8605G>C