Canonical Allele Identifier: PA239839
Gene: STIL HGNC NCBI

Linked Data

ClinVar Variation Id: 160052
ClinVar RCV Id: RCV000174311 RCV000210579 RCV000454157 RCV000513904 RCV000986319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041631.1:p.Leu485Phe
CA239838
NM_001048166.1:c.1455G>C
CA340248096
NM_001048166.1:c.1455G>T