Canonical Allele Identifier: PA2827062019
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1632880
ClinVar RCV Id: RCV002119341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Arg59Cys
CA5459597
NM_001320961.2:c.175C>T