Canonical Allele Identifier: PA891856438
Gene: SRPX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 566880
ClinVar RCV Id: RCV000686809 RCV004026247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055282.1:p.Arg413His
CA10469690
NM_014467.3:c.1238G>A