Canonical Allele Identifier: PA2828488782
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 523399
ClinVar RCV Id: RCV000626741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358376.1:p.Val272Met
CA350630384
NM_001371447.1:c.814G>A