Canonical Allele Identifier: PA1139690234
Gene: MAT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 851162
ClinVar RCV Id: RCV001055501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000420.1:p.Arg292His
CA5576683
NM_000429.3:c.875G>A