Allele Registry

Canonical Allele Identifier: PA296171

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000158040

RCV003539802

ClinVar Variation:

180912

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Val64Phe	CA296169 NM_030662.4:c.190G>T