Canonical Allele Identifier: PA2828490834
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_001358385.1:p.Val186Met
CA117999
NM_001371456.1:c.556G>A