Canonical Allele Identifier: PA227735
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004174.1:p.Leu567Phe
CA227734
NM_004183.3:c.1699C>T