Allele Registry

Canonical Allele Identifier: PA117988

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000006538

ClinVar Variation:

6163

HGVS (amino-acid)	Matching Registered Transcripts
NP_004319.1:p.Ser277Asn	CA117984 NM_004328.5:c.830G>A