Canonical Allele Identifier: PA288596
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128188
ClinVar RCV Id: RCV000116157 RCV000212335 RCV003460838
ClinVar Variation Id: 570962
ClinVar RCV Id: RCV000691968 RCV001190188 RCV002282331 RCV003492131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1138Tyr
CA288594
NM_032043.3:c.3412G>T
CA891843743
NM_032043.3:c.3411_3412delinsCT