Canonical Allele Identifier: PA1139700508
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 834058
ClinVar RCV Id: RCV001034615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Gln58His
CA392929256
NM_002755.4:c.174G>C
CA392929258
NM_002755.4:c.174G>T