Canonical Allele Identifier: PA341157
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_001158182.1:p.His42Arg
CA341155
NM_001164710.2:c.125A>G