Canonical Allele Identifier: PA916057076
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40844
ClinVar RCV Id: RCV000813491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Arg397His
CA9090683
NM_030662.4:c.1190G>A