Canonical Allele Identifier: PA916017909
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 209161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Asn787Ser
CA250356
NM_001291860.2:c.2360A>G