Canonical Allele Identifier: PA113442
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 11979
ClinVar RCV Id: RCV000012759 RCV003230357 RCV001090581
ClinVar Variation Id: 2581425
ClinVar RCV Id: RCV003331830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Arg320His
CA341159
NM_000481.4:c.959G>A
CA2582342856
NM_000481.4:c.954_959delinsAAGGCA