Allele Registry

Canonical Allele Identifier: PA296135

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000158025

RCV000466246

RCV000788004

RCV000824948

RCV001849290

ClinVar Variation:

40818

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Arg231Leu	CA296133 NM_030662.4:c.692G>T