Canonical Allele Identifier: PA645396235
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Val2116Met
CA671591
NM_005529.7:c.6346G>A