Canonical Allele Identifier: PA645396191
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_005520.4:p.Gly1635Arg
CA672124
NM_005529.7:c.4903G>A
CA338949833
NM_005529.7:c.4903G>C