Allele Registry

Canonical Allele Identifier: PA176711

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000151011

ClinVar Variation:

163960

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Phe57Ile	CA176709 NM_030662.4:c.169T>A