Canonical Allele Identifier: PA2828489372
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2178063
ClinVar RCV Id: RCV002588500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358378.1:p.Leu243Val
CA350629735
NM_001371449.1:c.727C>G