Canonical Allele Identifier: PA116910
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116427.1:p.Asn152Ser
CA116909
NM_001122955.4:c.455A>G