Canonical Allele Identifier: PA915988669
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 430735
ClinVar RCV Id: RCV000495928 RCV003230522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158183.1:p.Ser61Leu
CA2398389
NM_001164711.2:c.182C>T