Canonical Allele Identifier: PA2827054542
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1986475
ClinVar RCV Id: RCV002786219
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307646.1:p.Trp62Cys
CA65808554
NM_001320717.2:c.186G>T
CA350625810
NM_001320717.2:c.186G>C