Allele Registry

Canonical Allele Identifier: PA2828488789

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000006538

ClinVar Variation:

6163

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358376.1:p.Ser277Asn	CA117984 NM_001371447.1:c.830G>A