Allele Registry

Canonical Allele Identifier: PA296111

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV000158006

ClinVar Variation:

40785

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Ile103Ser	CA296109 NM_002755.4:c.308T>G