Allele Registry

Canonical Allele Identifier: PA2828472765

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000006539

RCV000665386

RCV001062637

RCV003472985

ClinVar Variation:

6164

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361014.1:p.Pro99Leu	CA117989 NM_001374085.1:c.296C>T