Canonical Allele Identifier: PA263571
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_000472.2:p.Ser77Leu
CA263569
NM_000481.4:c.230C>T