Canonical Allele Identifier: PA2826441389
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 625207
ClinVar RCV Id: RCV000778592 RCV000850204 RCV001003574 RCV001003575 RCV001855960 RCV003472287
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244273.1:p.Arg90Cys
CA2109634
NM_001257344.2:c.268C>T