Canonical Allele Identifier: PA263564
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 56226
ClinVar RCV Id: RCV000049638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Gly47Trp
CA263562
NM_000481.4:c.139G>T