Canonical Allele Identifier: PA2580473072
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2081253
ClinVar RCV Id: RCV002994141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Ala399Val
CA304445692
NM_030662.4:c.1196C>T