Canonical Allele Identifier: PA645386135
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 390155
ClinVar RCV Id: RCV000441325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116427.1:p.Val257Glu
CA16606265
NM_001122955.4:c.770T>A