Canonical Allele Identifier: PA2827062020
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397583
ClinVar RCV Id: RCV001906201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Arg59His
CA5459598
NM_001320961.2:c.176G>A