Allele Registry

Canonical Allele Identifier: PA2828490782

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000480400

ClinVar Variation:

423549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358385.1:p.Leu113Phe	CA16617468 NM_001371456.1:c.337C>T