Canonical Allele Identifier: PA2826850169
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99735
ClinVar RCV Id: RCV000086150 RCV000763263 RCV000787543 RCV001073491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287716.1:p.Arg158Cys
CA227795
NM_001300787.2:c.472C>T