Canonical Allele Identifier: PA916043826
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350520.1:p.Ala89Val
CA227785
NM_001363591.2:c.266C>T