Canonical Allele Identifier: PA915988739
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 531771
ClinVar RCV Id: RCV000638278 RCV001312022 RCV002529876 RCV003155257 RCV003492123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158184.1:p.Val212Ala
CA2398293
NM_001164712.2:c.635T>C