Canonical Allele Identifier: PA2741894680
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2901688
ClinVar RCV Id: RCV003654724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Ile216Thr
CA392936380
NM_002755.4:c.647T>C