Canonical Allele Identifier: PA137934
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 46234
ClinVar RCV Id: RCV003764692 RCV000039479
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Val131Met
CA137932
NM_030662.4:c.391G>A