Canonical Allele Identifier: PA2828487780
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6174
ClinVar RCV Id: RCV000006550 RCV000521027 RCV000674245 RCV003472991
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358372.1:p.Arg183Cys
CA118041
NM_001371443.1:c.547C>T