Canonical Allele Identifier: PA2827062024
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2099713
ClinVar RCV Id: RCV003023151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Val76Ala
CA376435825
NM_001320961.2:c.227T>C