Canonical Allele Identifier: PA891861735
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 567295
ClinVar RCV Id: RCV000687331 RCV002493153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116427.1:p.Pro258Leu
CA6053454
NM_001122955.4:c.773C>T