Canonical Allele Identifier: PA916017965
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Phe1498Ile
CA672259
NM_001291860.2:c.4492T>A