Canonical Allele Identifier: PA296101
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180896
ClinVar RCV Id: RCV000680291 RCV001857557 RCV002433694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Val93Ile
CA296099
NM_002755.4:c.277G>A