Canonical Allele Identifier: PA318812
Gene: SRPX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207393
ClinVar RCV Id: RCV000189571 RCV001351560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055282.1:p.Arg298His
CA318811
NM_014467.3:c.893G>A