Canonical Allele Identifier: PA2580242532
Gene: XIAP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365521.1:p.Glu476Asp
CA10508190
NM_001378592.1:c.1428A>C
CA414128157
NM_001378592.1:c.1428A>T