Canonical Allele Identifier: PA2828472881
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361014.1:p.Arg183Cys
CA118041
NM_001374085.1:c.547C>T