Canonical Allele Identifier: PA2828099087
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99780
ClinVar RCV Id: RCV000086199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350521.1:p.Arg374Thr
CA227852
NM_001363592.1:c.1121G>C