Allele Registry

Canonical Allele Identifier: PA2580472902

Gene: MAP2K2 HGNC NCBI

ClinVar RCV:

RCV002351129

ClinVar Variation:

1734825

HGVS (amino-acid)	Matching Registered Transcripts
NP_109587.1:p.Asn126Ser	CA403391504 NM_030662.4:c.377A>G