Allele Registry

Canonical Allele Identifier: PA658829292

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV000680037

ClinVar Variation:

40742

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Pro124Thr	CA392930699 NM_002755.4:c.370C>A