Canonical Allele Identifier: PA106890
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13351
ClinVar RCV Id: RCV000043672 RCV000208757 RCV000207506 RCV000541525 RCV000623321 RCV000763362 RCV001197351 RCV003450638 RCV004532347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Tyr130Cys
CA280036
NM_002755.4:c.389A>G