Canonical Allele Identifier: PA891849050
Gene: MAT1A HGNC NCBI
ClinVar RCV:
RCV000698221
ClinVar Variation:
575881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000420.1:p.Arg249Trp
CA5576723
NM_000429.3:c.745C>T