Canonical Allele Identifier: PA645420112
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 346037
ClinVar RCV Id: RCV000398839 RCV000710536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Ala51Val
CA2398463
NM_000481.4:c.152C>T