Canonical Allele Identifier: PA2826849870
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517426
ClinVar RCV Id: RCV002041079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287715.1:p.Trp251_Asn252delinsCysTyr
CA2573147315
NM_001300786.2:c.753_754delinsCT