Canonical Allele Identifier: PA296124
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40755
ClinVar RCV Id: RCV000158012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Ser244Ala
CA296122
NM_002755.4:c.730T>G