Canonical Allele Identifier: PA2828490258
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 126497
ClinVar RCV Id: RCV000114392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358382.1:p.Tyr134Asn
CA151154
NM_001371453.1:c.400T>A