Allele Registry

Canonical Allele Identifier: PA296168

Gene: MAP2K2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000158037

RCV000417753

RCV000428429

RCV000429600

RCV000438529

RCV000702132

RCV003447507

ClinVar Variation:

180911

376449

578970

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Phe57Leu	CA296166 NM_030662.4:c.169T>C CA16602884 NM_030662.4:c.171T>G CA403392731 NM_030662.4:c.171T>A