Canonical Allele Identifier: PA2828488308
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 214160
ClinVar RCV Id: RCV000197059 RCV000415034 RCV000623904 RCV000675122 RCV001810436 RCV003474948
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358375.1:p.Arg69Cys
CA321501
NM_001371446.1:c.205C>T