Allele Registry

Canonical Allele Identifier: PA2828489601

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000049826

ClinVar Variation:

56413

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358379.1:p.Arg144Gln	CA144345 NM_001371450.1:c.431G>A