Canonical Allele Identifier: PA256148
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 11975
ClinVar RCV Id: RCV000012755 RCV000622444 RCV003230354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158182.1:p.Gly47Arg
CA256146
NM_001164710.2:c.139G>A
CA352791256
NM_001164710.2:c.139G>C