Canonical Allele Identifier: PA296135
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40818
ClinVar RCV Id: RCV000158025 RCV000788004 RCV000824948 RCV000466246 RCV001849290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Arg231Leu
CA296133
NM_030662.4:c.692G>T