Allele Registry

Canonical Allele Identifier: PA180733

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000154387

ClinVar Variation:

40792

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Pro128Arg	CA180731 NM_030662.4:c.383C>G