Canonical Allele Identifier: PA2828489890
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6163
ClinVar RCV Id: RCV000006538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358380.1:p.Ser157Asn
CA117984
NM_001371451.1:c.470G>A