Allele Registry

Canonical Allele Identifier: PA296114

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV000505738

RCV001089756

RCV001385117

RCV001526460

ClinVar Variation:

40741

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.His119Tyr	CA296112 NM_002755.4:c.355C>T