Canonical Allele Identifier: PA2828098712
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350521.1:p.Thr6Pro
CA227736
NM_001363592.1:c.16A>C