Allele Registry

Canonical Allele Identifier: PA645425778

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV000444084

ClinVar Variation:

376180

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Val35Met	CA16602635 NM_030662.4:c.103G>A