Canonical Allele Identifier: PA341162
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 11979
ClinVar RCV Id: RCV000012759 RCV003230357 RCV001090581
ClinVar Variation Id: 2581425
ClinVar RCV Id: RCV003331830
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158182.1:p.Arg276His
CA341159
NM_001164710.2:c.827G>A
CA2582342856
NM_001164710.2:c.822_827delinsAAGGCA