Canonical Allele Identifier: PA231531
Gene: SRPX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 130374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055282.1:p.Arg458Gln
CA231530
NM_014467.3:c.1373G>A