Allele Registry

Canonical Allele Identifier: PA296124

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV000158012

ClinVar Variation:

40755

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Ser244Ala	CA296122 NM_002755.4:c.730T>G