Canonical Allele Identifier: PA107056
Gene: MAT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2429436
ClinVar RCV Id: RCV003126373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000420.1:p.Arg356Gln
CA5576621
NM_000429.3:c.1067G>A