Canonical Allele Identifier: PA658805402
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40740
ClinVar RCV Id: RCV001813305 RCV004018722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Leu115Val
CA392930543
NM_002755.4:c.343C>G