Canonical Allele Identifier: PA2826676157
Gene: STIL HGNC NCBI

Linked Data

ClinVar Variation Id: 160052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269868.1:p.Leu438Phe
CA239838
NM_001282939.1:c.1314G>C
CA340248096
NM_001282939.1:c.1314G>T