Canonical Allele Identifier: PA2828487998
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1302936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358373.1:p.Arg69His
CA2109622
NM_001371444.1:c.206G>A