Canonical Allele Identifier: PA2827062013
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525745
ClinVar RCV Id: RCV002036917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Met49Lys
CA376435642
NM_001320961.2:c.146T>A