Canonical Allele Identifier: PA2826441359
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 283781
ClinVar RCV Id: RCV000266879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244273.1:p.His70Arg
CA2109626
NM_001257344.2:c.209A>G