Canonical Allele Identifier: PA645420117
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 430735
ClinVar RCV Id: RCV000495928 RCV003230522
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Ser117Leu
CA2398389
NM_000481.4:c.350C>T