Canonical Allele Identifier: PA2828490005
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 551244
ClinVar RCV Id: RCV000666246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358381.1:p.Arg36_Val38del
CA539839958
NM_001371452.1:c.106_114del