Canonical Allele Identifier: PA2580113627
Gene: MAT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2040728
ClinVar RCV Id: RCV002890755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000420.1:p.Ala281Thr
CA377360764
NM_000429.3:c.841G>A