Canonical Allele Identifier: PA2828487697
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2041499
ClinVar RCV Id: RCV002903015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358372.1:p.Arg73Gly
CA65808578
NM_001371443.1:c.217C>G