Canonical Allele Identifier: PA2826000858
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 56229
ClinVar RCV Id: RCV000049641 RCV002274890
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158182.1:p.Ser77Leu
CA263569
NM_001164710.2:c.230C>T