Canonical Allele Identifier: PA2828487998
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1302936
ClinVar RCV Id: RCV001756435 RCV002496067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358373.1:p.Arg69His
CA2109622
NM_001371444.1:c.206G>A