Canonical Allele Identifier: PA2828098842
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99702
ClinVar RCV Id: RCV000086113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350521.1:p.Arg92Ser
CA227754
NM_001363592.1:c.274C>A