Canonical Allele Identifier: PA2826850145
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287716.1:p.Ala135Val
CA227785
NM_001300787.2:c.404C>T