Allele Registry

Canonical Allele Identifier: PA180916

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000154524

RCV000681198

RCV001172272

RCV003162628

RCV003416007

ClinVar Variation:

177876

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Pro269Arg	CA180914 NM_030662.4:c.806C>G