Canonical Allele Identifier: PA915969870
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 667260
ClinVar RCV Id: RCV000825953 RCV004029192
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Lys88Arg
CA7623882
NM_002755.4:c.263A>G