Canonical Allele Identifier: PA2825698620
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773320
ClinVar RCV Id: RCV002396894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124174.2:p.Tyr49Cys
CA6053620
NM_001130702.2:c.146A>G