Canonical Allele Identifier: PA2828490569
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2178063
ClinVar RCV Id: RCV002588500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358384.1:p.Leu76Val
CA350629735
NM_001371455.1:c.226C>G