Canonical Allele Identifier: PA2580473057
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2199936
ClinVar RCV Id: RCV002625219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Arg371Leu
CA403381137
NM_030662.4:c.1112G>T