Canonical Allele Identifier: PA2825186409
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2126778
ClinVar RCV Id: RCV003051832
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Val59Met
CA2398458
NM_000481.4:c.175G>A