Canonical Allele Identifier: PA1139765093
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 837895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Gly393Ser
CA9090687
NM_030662.4:c.1177G>A