Canonical Allele Identifier: PA2827301621
Gene: AICDA HGNC NCBI

Linked Data

ClinVar Variation Id: 5122
ClinVar RCV Id: RCV000005429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317272.1:p.Arg24Trp
CA117266
NM_001330343.2:c.70C>T