Canonical Allele Identifier: PA645396321
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_005520.4:p.Ala3396Val
CA670199
NM_005529.7:c.10187C>T