Canonical Allele Identifier: PA2828488708
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358376.1:p.Arg184Cys
CA118026
NM_001371447.1:c.550C>T