Allele Registry

Canonical Allele Identifier: PA645423244

Gene: MAP2K1 HGNC NCBI

ClinVar Allele:

363054

ClinVar RCV:

RCV000422377

RCV005252499

ClinVar Variation:

376175

3775508

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Phe129Leu	CA16602630 NM_002755.4:c.385T>C CA392930778 NM_002755.4:c.387C>A CA392930781 NM_002755.4:c.387C>G