Canonical Allele Identifier: PA2826849778
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287715.1:p.Tyr167Cys
CA115733
NM_001300786.2:c.500A>G