Canonical Allele Identifier: PA916018105
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 289408
ClinVar RCV Id: RCV000369617 RCV000726320 RCV001096488 RCV001096489 RCV002522005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Ala3397Val
CA670199
NM_001291860.2:c.10190C>T