Canonical Allele Identifier: PA209688
Gene: SRPX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 139323
ClinVar RCV Id: RCV000195094 RCV000424626 RCV001085267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055282.1:p.His154Asp
CA209687
NM_014467.3:c.460C>G