Canonical Allele Identifier: PA165628
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141499
ClinVar RCV Id: RCV000130056 RCV000699539 RCV000663220 RCV001194712 RCV001255230 RCV002273958 RCV003460909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg848His
CA165626
NM_032043.3:c.2543G>A