Canonical Allele Identifier: PA2573096967
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320470
ClinVar RCV Id: RCV001776449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116056.3:p.Ser45Pro
CA380970542
NM_032667.6:c.133T>C