Canonical Allele Identifier: PA2826849868
Gene: BEST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2820519
ClinVar RCV Id: RCV003709233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001287715.1:p.Trp251Arg
CA380846199
NM_001300786.2:c.751T>A
CA380846200
NM_001300786.2:c.751T>C