Canonical Allele Identifier: PA2580154308
Gene: AANAT HGNC NCBI

Linked Data

ClinVar Variation Id: 2400665
ClinVar RCV Id: RCV004238489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160051.1:p.Arg176Trp
CA294178169
NM_001166579.2:c.526C>T