Canonical Allele Identifier: PA2826440950
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244272.1:p.Arg184Cys
CA118026
NM_001257343.2:c.550C>T