Canonical Allele Identifier: PA180897
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40843
ClinVar RCV Id: RCV000200611 RCV000154509 RCV000680296 RCV000824952 RCV001334284 RCV002354182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Arg388Trp
CA180895
NM_030662.4:c.1162C>T