Canonical Allele Identifier: PA263588
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_000472.2:p.Arg296His
CA263586
NM_000481.4:c.887G>A