Canonical Allele Identifier: PA645396255
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Thr2511Ile
CA671143
NM_005529.7:c.7532C>T