Allele Registry

Canonical Allele Identifier: PA296141

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000158027

RCV000522446

RCV000781517

RCV000990136

RCV003952390

ClinVar Variation:

40824

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Lys273Arg	CA296139 NM_030662.4:c.818A>G