Canonical Allele Identifier: PA184281
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 179368
ClinVar RCV Id: RCV000156157 RCV000654956 RCV002223794 RCV004019873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Arg108Gln
CA184279
NM_002755.4:c.323G>A