Canonical Allele Identifier: PA137968
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 46242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Val262Ile
CA137966
NM_030662.4:c.784G>A