Canonical Allele Identifier: PA2829061484
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 390155
ClinVar RCV Id: RCV000441325
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372956.1:p.Val257Glu
CA16606265
NM_001386027.1:c.770T>A