Canonical Allele Identifier: PA2827301688
Gene: AICDA HGNC NCBI

Linked Data

ClinVar Variation Id: 5124
ClinVar RCV Id: RCV000005431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317272.1:p.Trp80Arg
CA117271
NM_001330343.2:c.238T>C
CA383819194
NM_001330343.2:c.238T>A