Canonical Allele Identifier: PA2828488108
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 551244
ClinVar RCV Id: RCV000666246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358373.1:p.Arg203_Val205del
CA539839958
NM_001371444.1:c.607_615del