Allele Registry

Canonical Allele Identifier: PA106872

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV000043673

RCV000158013

RCV000207493

RCV000211725

RCV001234104

ClinVar Variation:

13352

40745

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Gly128Val	CA280038 NM_002755.4:c.383G>T CA296125 NM_002755.4:c.383_384delinsTT