Canonical Allele Identifier: PA2828487696
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2161937
ClinVar RCV Id: RCV003089752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358372.1:p.Arg73His
CA2109628
NM_001371443.1:c.218G>A