Canonical Allele Identifier: PA349932
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116427.1:p.Arg350Gln
CA349931
NM_001122955.4:c.1049G>A