Canonical Allele Identifier: PA272692
Gene: STIL HGNC NCBI

Linked Data

ClinVar Variation Id: 160068
ClinVar RCV Id: RCV000147699 RCV001092679
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041631.1:p.His156Arg
CA272691
NM_001048166.1:c.467A>G