Canonical Allele Identifier: PA118002
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6166
ClinVar RCV Id: RCV000006541 RCV001851699 RCV003472986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244273.1:p.Val353Met
CA117999
NM_001257344.2:c.1057G>A