Canonical Allele Identifier: PA645396288
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295772
ClinVar RCV Id: RCV000298518 RCV000355753 RCV000992149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Thr2859Met
CA670735
NM_005529.7:c.8576C>T