Allele Registry

Canonical Allele Identifier: PA658805402

Gene: MAP2K1 HGNC NCBI

ClinVar Allele:

49210

ClinVar RCV:

RCV001813305

RCV004018722

ClinVar Variation:

40740

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Leu115Val	CA392930543 NM_002755.4:c.343C>G