Canonical Allele Identifier: PA2825186426
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1044553
ClinVar RCV Id: RCV001348813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Thr66Ala
CA352791139
NM_000481.4:c.196A>G