Canonical Allele Identifier: PA2825698665
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 476810
ClinVar RCV Id: RCV000536990 RCV000789082 RCV001270682 RCV002284966 RCV003311850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124174.2:p.Ser90Trp
CA380968385
NM_001130702.2:c.269C>G