Canonical Allele Identifier: PA2826849620
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99702
ClinVar RCV Id: RCV000086113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287715.1:p.Arg32Ser
CA227754
NM_001300786.2:c.94C>A