Canonical Allele Identifier: PA913199555
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 549715
ClinVar RCV Id: RCV000754918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116427.1:p.Glu246delinsAspArg
CA6053488
NM_001122955.4:c.737_738insCCG