Allele Registry

Canonical Allele Identifier: PA279995

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV000037590

RCV001582510

RCV001787832

RCV003539771

ClinVar Variation:

44587

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Leu42Phe	CA279993 NM_002755.4:c.124C>T