Canonical Allele Identifier: PA2828098952
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350521.1:p.Ala195Val
CA227785
NM_001363592.1:c.584C>T