Canonical Allele Identifier: PA272681
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_001041631.1:p.Val1023Leu
CA272679
NM_001048166.1:c.3067G>T
CA340235964
NM_001048166.1:c.3067G>C