Allele Registry

Canonical Allele Identifier: PA2741894698

Gene: MAP2K1 HGNC NCBI

ClinVar Variation Id: 2997336

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Phe371Leu	CA392938956 NM_002755.4:c.1111T>C CA392938967 NM_002755.4:c.1113T>A CA392938969 NM_002755.4:c.1113T>G