Canonical Allele Identifier: PA180892
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 177868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Tyr134Cys
CA180890
NM_030662.4:c.401A>G