Canonical Allele Identifier: PA201277
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 194641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Val692Met
CA201276
NM_005529.7:c.2074G>A