Canonical Allele Identifier: PA913200207
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40847
ClinVar RCV Id: RCV000781516 RCV000866602 RCV001610309 RCV001813319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Val400Met
CA9090680
NM_030662.4:c.1198G>A