Canonical Allele Identifier: PA2827301686
Gene: AICDA HGNC NCBI

Linked Data

ClinVar Variation Id: 2047339
ClinVar RCV Id: RCV002926822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317272.1:p.Val78Leu
CA383819220
NM_001330343.2:c.232G>C