Canonical Allele Identifier: PA2499278719
Gene: SRPX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1013627
ClinVar RCV Id: RCV001312244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055282.1:p.Thr377Ala
CA413915540
NM_014467.3:c.1129A>G