Allele Registry

Canonical Allele Identifier: PA2741991669

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV003655714

ClinVar Variation:

2815389

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Ala56Thr	CA403392747 NM_030662.4:c.166G>A