Canonical Allele Identifier: PA134624
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40756
ClinVar RCV Id: RCV000037602 RCV000519375 RCV001719721 RCV004018723 RCV004532502
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Ala283Val
CA134622
NM_002755.4:c.848C>T