Canonical Allele Identifier: PA916043839
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99775
ClinVar RCV Id: RCV000086194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350521.1:p.Met370Val
CA227847
NM_001363592.1:c.1108A>G