Canonical Allele Identifier: PA2827062014
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2110437
ClinVar RCV Id: RCV003042353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Asp52Gly
CA376435668
NM_001320961.2:c.155A>G