Allele Registry

Canonical Allele Identifier: PA296159

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000158034

RCV000546588

RCV000781515

ClinVar Variation:

40842

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Arg371Gln	CA296157 NM_030662.4:c.1112G>A