Canonical Allele Identifier: PA2828490062
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 523399
ClinVar RCV Id: RCV000626741
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358381.1:p.Val105Met
CA350630384
NM_001371452.1:c.313G>A