Allele Registry

Canonical Allele Identifier: PA3057321853

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV004812965

ClinVar Variation:

3390795

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Ile111Thr	CA392930464 NM_002755.4:c.332T>C