Canonical Allele Identifier: PA2827062030
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1365710
ClinVar RCV Id: RCV001929934

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Asn93Asp
CA376435935
NM_001320961.2:c.277A>G