Canonical Allele Identifier: PA245019
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 197080
ClinVar RCV Id: RCV000178005 RCV000191093 RCV001099320 RCV000991336 RCV004537456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Thr1639Met
CA245018
NM_005529.7:c.4916C>T