Canonical Allele Identifier: PA2826001361
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 56239
ClinVar RCV Id: RCV000049651 RCV000436156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158183.1:p.Arg240His
CA263586
NM_001164711.2:c.719G>A