Canonical Allele Identifier: PA2828488625
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6167
ClinVar RCV Id: RCV000006542 RCV000519547 RCV000983982 RCV002476936 RCV003472987
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358376.1:p.Ser78Gly
CA118004
NM_001371447.1:c.232A>G