Allele Registry

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Canonical Allele Identifier: PA2826440732

Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1120065

ClinVar RCV Id: RCV001449705 RCV001832578 RCV002476767

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244272.1:p.Ser65Arg	CA2109617 NM_001257343.2:c.193A>C CA350625828 NM_001257343.2:c.195C>A CA350625829 NM_001257343.2:c.195C>G