Canonical Allele Identifier: PA2826676269
Gene: STIL HGNC NCBI

Linked Data

ClinVar Variation Id: 297551
ClinVar RCV Id: RCV000376610 RCV000912683 RCV003910086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269868.1:p.Ser1107Phe
CA841961
NM_001282939.1:c.3320C>T