Allele Registry

Canonical Allele Identifier: PA891856353

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000694725

RCV001756198

ClinVar Variation:

573141

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Ser127Leu	CA403391488 NM_030662.4:c.380C>T