Canonical Allele Identifier: PA134603
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 44588
ClinVar RCV Id: RCV000158005 RCV000522848 RCV001813322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Leu92Arg
CA134601
NM_002755.4:c.275T>G