Canonical Allele Identifier: PA117987
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6163
ClinVar RCV Id: RCV000006538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244273.1:p.Ser277Asn
CA117984
NM_001257344.2:c.830G>A