Canonical Allele Identifier: PA2826001339
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 346031
ClinVar RCV Id: RCV000373179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158183.1:p.Asn219Lys
CA2398230
NM_001164711.2:c.657T>A
CA352789767
NM_001164711.2:c.657T>G