Canonical Allele Identifier: PA2828490697
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358385.1:p.Arg16Cys
CA118041
NM_001371456.1:c.46C>T