Canonical Allele Identifier: PA2826850346
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 972579
ClinVar RCV Id: RCV001248641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287716.1:p.Pro286Ala
CA380846262
NM_001300787.2:c.856C>G