Canonical Allele Identifier: PA2828488905
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6168
ClinVar RCV Id: RCV000006543 RCV001851700 RCV003472988
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358377.1:p.Arg45Cys
CA118010
NM_001371448.1:c.133C>T