Canonical Allele Identifier: PA2827062000
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3123032
ClinVar RCV Id: RCV004408402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Ser5Ile
CA205307067
NM_001320961.2:c.14G>T