Canonical Allele Identifier: PA645386133
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 305179
ClinVar RCV Id: RCV000265700 RCV000309083 RCV001859815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116427.1:p.Ala249Ser
CA10638912
NM_001122955.4:c.745G>T