Canonical Allele Identifier: PA2828489566
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6164
ClinVar RCV Id: RCV000006539 RCV000665386 RCV001062637 RCV003472985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358379.1:p.Pro99Leu
CA117989
NM_001371450.1:c.296C>T