Allele Registry

Canonical Allele Identifier: PA137934

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000039479

RCV003764692

ClinVar Variation:

46234

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Val131Met	CA137932 NM_030662.4:c.391G>A