Canonical Allele Identifier: PA2580211427
Gene: SAP25 HGNC NCBI

Linked Data

ClinVar Variation Id: 2298443
ClinVar RCV Id: RCV004147604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335609.1:p.Arg224His
CA368522884
NM_001348680.2:c.671G>A