Canonical Allele Identifier: PA915969811
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 666418
ClinVar RCV Id: RCV000824934

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Gln46Leu
CA392929105
NM_002755.4:c.137A>T