Canonical Allele Identifier: PA2573078566
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 549715
ClinVar RCV Id: RCV000754918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372957.1:p.Glu246delinsAspArg
CA6053488
NM_001386028.1:c.737_738insCCG