Canonical Allele Identifier: PA916014083
Gene: STIL HGNC NCBI

Linked Data

ClinVar Variation Id: 160061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269867.1:p.Val976Leu
CA272679
NM_001282938.1:c.2926G>T
CA340235964
NM_001282938.1:c.2926G>C