Allele Registry

Canonical Allele Identifier: PA2573291482

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV002028395

ClinVar Variation:

1495968

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Gly132Val	CA403391424 NM_030662.4:c.395G>T