Canonical Allele Identifier: PA2827062012
Gene: MAP3K8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350193
ClinVar RCV Id: RCV002051259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307890.1:p.Met47Ile
CA5459593
NM_001320961.2:c.141G>A
CA376435631
NM_001320961.2:c.141G>C
CA376435632
NM_001320961.2:c.141G>T