Canonical Allele Identifier: PA2829061647
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1970637
ClinVar RCV Id: RCV002735429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372957.1:p.Tyr117Cys
CA380970435
NM_001386028.1:c.350A>G