Canonical Allele Identifier: PA263568
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 56228
ClinVar RCV Id: RCV000049640 RCV001090584 RCV002251953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Arg73Cys
CA263566
NM_000481.4:c.217C>T