Canonical Allele Identifier: PA2829061379
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1389256
ClinVar RCV Id: RCV001887090
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372956.1:p.Thr123Ile
CA380970334
NM_001386027.1:c.368C>T