Canonical Allele Identifier: PA2828489227
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1986475
ClinVar RCV Id: RCV002786219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358378.1:p.Trp62Cys
CA65808554
NM_001371449.1:c.186G>T
CA350625810
NM_001371449.1:c.186G>C