Canonical Allele Identifier: PA2829061481
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2510841
ClinVar RCV Id: RCV003240265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372956.1:p.Ser255Leu
CA6053482
NM_001386027.1:c.764C>T