Canonical Allele Identifier: PA2580472958
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1757301
ClinVar RCV Id: RCV002378338 RCV003741308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Arg238Trp
CA403387959
NM_030662.4:c.712C>T