Canonical Allele Identifier: PA2573082220
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1316067
ClinVar RCV Id: RCV001757514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Gly210Arg
CA392936300
NM_002755.4:c.628G>A
CA392936302
NM_002755.4:c.628G>C