Canonical Allele Identifier: PA2827062002
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1473251
ClinVar RCV Id: RCV002005205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Gly7Glu
CA5459568
NM_001320961.2:c.20G>A