Canonical Allele Identifier: PA2828099131
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 166747
ClinVar RCV Id: RCV000152854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350522.1:p.Met12Arg
CA233534
NM_001363593.2:c.35T>G