Canonical Allele Identifier: PA113485
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 11976
ClinVar RCV Id: RCV000012756 RCV003230355
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.His42Arg
CA341155
NM_000481.4:c.125A>G