Canonical Allele Identifier: PA117993
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6164
ClinVar RCV Id: RCV000006539 RCV000665386 RCV001062637 RCV003472985
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004319.1:p.Pro99Leu
CA117989
NM_004328.5:c.296C>T