Canonical Allele Identifier: PA288590
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128186
ClinVar RCV Id: RCV000116155 RCV000204181 RCV000410336 RCV000409119 RCV000214821 RCV001194197 RCV001354313 RCV003315658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1111Gln
CA288588
NM_032043.3:c.3331G>C