Canonical Allele Identifier: PA2830087579
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2698778
ClinVar RCV Id: RCV003582211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116056.3:p.Asp186Asn
CA380962568
NM_032667.6:c.556G>A