Canonical Allele Identifier: PA915988793
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_001158184.1:p.Arg296His
CA263586
NM_001164712.2:c.887G>A