Canonical Allele Identifier: PA645420135
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 346029
ClinVar RCV Id: RCV000330007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Val321Met
CA2398193
NM_000481.4:c.961G>A