Canonical Allele Identifier: PA2741894698
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2997336
ClinVar RCV Id: RCV003851455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Phe371Leu
CA392938956
NM_002755.4:c.1111T>C
CA392938967
NM_002755.4:c.1113T>A
CA392938969
NM_002755.4:c.1113T>G