Canonical Allele Identifier: PA2830087595
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 390155
ClinVar RCV Id: RCV000441325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116056.3:p.Val193Glu
CA16606265
NM_032667.6:c.578T>A