Canonical Allele Identifier: PA2826001558
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 531768
ClinVar RCV Id: RCV000638275 RCV003243225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158184.1:p.Ala146Thr
CA2398372
NM_001164712.2:c.436G>A