Canonical Allele Identifier: PA107076
Gene: MAT1A HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000420.1:p.Gly336Arg
CA114842
NM_000429.3:c.1006G>A
CA377360417
NM_000429.3:c.1006G>C