Allele Registry

Canonical Allele Identifier: PA1139700523

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV001063772

ClinVar Variation:

857990

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Glu69Lys	CA392929332 NM_002755.4:c.205G>A