Canonical Allele Identifier: PA913198967
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 625207
ClinVar RCV Id: RCV000778592 RCV000850204 RCV001003574 RCV001003575 RCV001855960 RCV003472287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004319.1:p.Arg90Cys
CA2109634
NM_004328.5:c.268C>T