Canonical Allele Identifier: PA2573078538
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 305184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372957.1:p.Gly44Asp
CA6053653
NM_001386028.1:c.131G>A