Canonical Allele Identifier: PA2827062032
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2428416
ClinVar RCV Id: RCV003120027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Met112Val
CA376436064
NM_001320961.2:c.334A>G