Canonical Allele Identifier: PA2826000805
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 531783
ClinVar RCV Id: RCV000638292 RCV003479181 RCV003937920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158182.1:p.Arg34His
CA2398472
NM_001164710.2:c.101G>A