Canonical Allele Identifier: PA118009
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6167
ClinVar RCV Id: RCV000006542 RCV000519547 RCV000983982 RCV002476936 RCV003472987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004319.1:p.Ser78Gly
CA118004
NM_004328.5:c.232A>G