Canonical Allele Identifier: PA2828490697
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6174
ClinVar RCV Id: RCV000006550 RCV000521027 RCV000674245 RCV003472991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358385.1:p.Arg16Cys
CA118041
NM_001371456.1:c.46C>T