Canonical Allele Identifier: PA2826675769
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_001269866.1:p.Val1005Leu
CA272679
NM_001282937.1:c.3013G>T
CA340235964
NM_001282937.1:c.3013G>C