Canonical Allele Identifier: PA2826440477
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 126497
ClinVar RCV Id: RCV000114392
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244271.1:p.Tyr301Asn
CA151154
NM_001257342.2:c.901T>A