Canonical Allele Identifier: PA2499278716
Gene: SRPX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1038364
ClinVar RCV Id: RCV001341660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055282.1:p.Thr219Ser
CA413935062
NM_014467.3:c.655A>T
CA413935076
NM_014467.3:c.656C>G