Canonical Allele Identifier: PA2825698795
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2698778
ClinVar RCV Id: RCV003582211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124174.2:p.Asp186Asn
CA380962568
NM_001130702.2:c.556G>A