Canonical Allele Identifier: PA2828099015
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99746
ClinVar RCV Id: RCV000086163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350521.1:p.Thr237Arg
CA227810
NM_001363592.1:c.710C>G