Canonical Allele Identifier: PA2829061487
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1707735
ClinVar RCV Id: RCV002286896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372956.1:p.Pro258Arg
CA380962330
NM_001386027.1:c.773C>G