Canonical Allele Identifier: PA354833
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222074
ClinVar RCV Id: RCV000207500 RCV002277569 RCV002515536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Lys59del
CA354831
NM_002755.4:c.175_177del