Canonical Allele Identifier: PA2826033412
Gene: AANAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3133743
ClinVar RCV Id: RCV004429029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160051.1:p.Asp145His
CA401161002
NM_001166579.2:c.433G>C