Canonical Allele Identifier: PA2829061467
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 581808
ClinVar RCV Id: RCV000705740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372956.1:p.Val227Phe
CA380963063
NM_001386027.1:c.679G>T