Allele Registry

Canonical Allele Identifier: PA296121

Gene: MAP2K1 HGNC NCBI

ClinVar Variation Id: 40752

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Met219Ile	CA296119 NM_002755.4:c.657G>C CA392936422 NM_002755.4:c.657G>A CA392936424 NM_002755.4:c.657G>T