Canonical Allele Identifier: PA2741991888
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2882490
ClinVar RCV Id: RCV003654568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Gly393Val
CA403380729
NM_030662.4:c.1178G>T