Canonical Allele Identifier: PA2580113625
Gene: MAT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1927181
ClinVar RCV Id: RCV002609747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000420.1:p.His277Tyr
CA5576691
NM_000429.3:c.829C>T