Canonical Allele Identifier: PA2580113644
Gene: MAT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2433652
ClinVar RCV Id: RCV003132600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000420.1:p.Tyr335His
CA5576637
NM_000429.3:c.1003T>C