Canonical Allele Identifier: PA915988762
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 462900
ClinVar RCV Id: RCV000533799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158184.1:p.Asp229His
CA352790066
NM_001164712.2:c.685G>C