Canonical Allele Identifier: PA2829061656
Gene: BSCL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1390835
ClinVar RCV Id: RCV001891203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372957.1:p.Val130Ala
CA380970188
NM_001386028.1:c.389T>C