Canonical Allele Identifier: PA2826850278
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99767
ClinVar RCV Id: RCV000086185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287716.1:p.Phe238Ser
CA227837
NM_001300787.2:c.713T>C