Canonical Allele Identifier: PA2826001035
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 56239
ClinVar RCV Id: RCV000049651 RCV000436156
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158182.1:p.Arg252His
CA263586
NM_001164710.2:c.755G>A