Canonical Allele Identifier: PA2827449209
Gene: SAP25 HGNC NCBI
ClinVar RCV:
RCV004291395
ClinVar Variation:
2514813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335609.1:p.Arg189Trp
CA163273628
NM_001348680.2:c.565C>T