Canonical Allele Identifier: PA658803668
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 531761
ClinVar RCV Id: RCV000638268 RCV001090580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Arg371His
CA2398140
NM_000481.4:c.1112G>A