Canonical Allele Identifier: PA916017977
Gene: HSPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295836
ClinVar RCV Id: RCV000263287 RCV000355506 RCV002522113 RCV002494920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Gly1636Arg
CA672124
NM_001291860.2:c.4906G>A
CA338949833
NM_001291860.2:c.4906G>C