Canonical Allele Identifier: PA2741907875
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_004174.1:p.Trp338Arg
CA380846199
NM_004183.3:c.1012T>A
CA380846200
NM_004183.3:c.1012T>C