Canonical Allele Identifier: PA916018172
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447542
ClinVar RCV Id: RCV000518544 RCV001095861 RCV001095862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Gly4346Arg
CA669145
NM_001291860.2:c.13036G>A
CA338908452
NM_001291860.2:c.13036G>C