Allele Registry

Canonical Allele Identifier: PA2828490080

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000114392

ClinVar Variation:

126497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358381.1:p.Tyr134Asn	CA151154 NM_001371452.1:c.400T>A