Canonical Allele Identifier: PA296138
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180906
ClinVar RCV Id: RCV000588108 RCV001857558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Pro269Leu
CA296136
NM_030662.4:c.806C>T