Canonical Allele Identifier: PA2826850274
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99763
ClinVar RCV Id: RCV000086181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287716.1:p.Asn236His
CA227833
NM_001300787.2:c.706A>C