Allele Registry

Canonical Allele Identifier: PA250290

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000023088

RCV000149835

RCV000413893

ClinVar Variation:

30170

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Gly132Asp	CA250288 NM_030662.4:c.395G>A