Canonical Allele Identifier: PA2827062029
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1498924
ClinVar RCV Id: RCV002035663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.His90Tyr
CA376435913
NM_001320961.2:c.268C>T