Allele Registry

Canonical Allele Identifier: PA137968

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000039493

RCV000519690

ClinVar Variation:

46242

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Val262Ile	CA137966 NM_030662.4:c.784G>A