Canonical Allele Identifier: PA2830087561
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045204
ClinVar RCV Id: RCV001349573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116056.3:p.Tyr184His
CA380962606
NM_032667.6:c.550T>C