Canonical Allele Identifier: PA916076751
Gene: MAP3K7 HGNC NCBI

Linked Data

ClinVar Variation Id: 422420
ClinVar RCV Id: RCV000478415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_663306.1:p.Ala107Thr
CA16618340
NM_145333.3:c.319G>A