Canonical Allele Identifier: PA2827021438
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 126497
ClinVar RCV Id: RCV000114392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305765.1:p.Tyr181Asn
CA151154
NM_001318836.2:c.541T>A