Canonical Allele Identifier: PA118013
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6168
ClinVar RCV Id: RCV000006543 RCV001851700 RCV003472988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244273.1:p.Arg45Cys
CA118010
NM_001257344.2:c.133C>T