Allele Registry

Canonical Allele Identifier: PA645423219

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV000423068

ClinVar Variation:

376195

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.His119Pro	CA16602650 NM_002755.4:c.356A>C