Canonical Allele Identifier: PA272680
Gene: STIL HGNC NCBI

Linked Data

ClinVar Variation Id: 160061
ClinVar RCV Id: RCV000147692 RCV000713535
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003026.2:p.Val1022Leu
CA272679
NM_003035.2:c.3064G>T
CA340235964
NM_003035.2:c.3064G>C