Canonical Allele Identifier: PA2826058796
Gene: SAP25 HGNC NCBI
ClinVar RCV:
RCV004291395
ClinVar Variation:
2514813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162153.2:p.Arg182Trp
CA163273628
NM_001168682.3:c.544C>T