Canonical Allele Identifier: PA318818
Gene: SRPX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207396
ClinVar RCV Id: RCV000189576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055282.1:p.Arg393Trp
CA318817
NM_014467.3:c.1177C>T