Canonical Allele Identifier: PA645425879
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40788
ClinVar RCV Id: RCV000285952 RCV002513331 RCV003488354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Ile97Met
CA9091061
NM_030662.4:c.291C>G