Allele Registry

Canonical Allele Identifier: PA916056886

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000807052

ClinVar Variation:

651646

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Asn126His	CA403391510 NM_030662.4:c.376A>C