Canonical Allele Identifier: PA2828098446
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99763
ClinVar RCV Id: RCV000086181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350520.1:p.Asn190His
CA227833
NM_001363591.2:c.568A>C