Canonical Allele Identifier: PA2580484711
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773320
ClinVar RCV Id: RCV002396894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116056.3:p.Tyr49Cys
CA6053620
NM_032667.6:c.146A>G