Canonical Allele Identifier: PA658816664
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530347
ClinVar RCV Id: RCV000636164 RCV001775935 RCV002343241 RCV003451522
ClinVar Variation Id: 1745212
ClinVar RCV Id: RCV002335884 RCV003454162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gln169His
CA400484345
NM_032043.3:c.507G>T
CA400484346
NM_032043.3:c.507G>C