Canonical Allele Identifier: PA2580263479
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2055758
ClinVar RCV Id: RCV002910125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Asp267Val
CA392937230
NM_002755.4:c.800A>T