Canonical Allele Identifier: PA2826271919
Gene: XIAP HGNC NCBI
ClinVar RCV:
RCV003051113
ClinVar Variation:
2142682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191330.1:p.Glu476Asp
CA10508190
NM_001204401.2:c.1428A>C
CA414128157
NM_001204401.2:c.1428A>T