Canonical Allele Identifier: PA2828489547
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2161937
ClinVar RCV Id: RCV003089752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358379.1:p.Arg73His
CA2109628
NM_001371450.1:c.218G>A