Canonical Allele Identifier: PA168448
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142473
ClinVar RCV Id: RCV000131607 RCV000222534 RCV000465039 RCV000662789 RCV000781166 RCV002288649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gln540Leu
CA168446
NM_032043.3:c.1619A>T