Canonical Allele Identifier: PA2829378927
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2686012
ClinVar RCV Id: RCV003991601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Ser212Thr
CA271671674
NM_002755.4:c.635G>C