Canonical Allele Identifier: PA092787
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99781
ClinVar RCV Id: RCV000086200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004174.1:p.Thr307Ala
CA227853
NM_004183.3:c.919A>G