Canonical Allele Identifier: PA1139700523
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 857990
ClinVar RCV Id: RCV001063772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Glu69Lys
CA392929332
NM_002755.4:c.205G>A