Allele Registry

Canonical Allele Identifier: PA296117

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV000158009

ClinVar Variation:

180901

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Glu138Lys	CA296115 NM_002755.4:c.412G>A