Canonical Allele Identifier: PA2826849590
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 837730
ClinVar RCV Id: RCV001039127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287715.1:p.Tyr12Asp
CA380833729
NM_001300786.2:c.34T>G