Canonical Allele Identifier: PA2826849879
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 972579
ClinVar RCV Id: RCV001248641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287715.1:p.Pro259Ala
CA380846262
NM_001300786.2:c.775C>G