Allele Registry

Canonical Allele Identifier: PA2828489902

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000114392

ClinVar Variation:

126497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358380.1:p.Tyr181Asn	CA151154 NM_001371451.1:c.541T>A