Canonical Allele Identifier: PA280001
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40747
ClinVar RCV Id: RCV000037596 RCV000623628 RCV001811234
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Tyr130His
CA279999
NM_002755.4:c.388T>C