Canonical Allele Identifier: PA2573078542
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 305182
ClinVar RCV Id: RCV000302313 RCV000398286 RCV003950023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372957.1:p.Leu62Phe
CA6053645
NM_001386028.1:c.184C>T