Canonical Allele Identifier: PA2741894679
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2905812
ClinVar RCV Id: RCV003654768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Gly213Arg
CA392936335
NM_002755.4:c.637G>C
CA392936338
NM_002755.4:c.637G>A