Canonical Allele Identifier: PA288593
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128187
ClinVar RCV Id: RCV000116156 RCV000212334 RCV000411633 RCV000587193 RCV000989979 RCV001354736 RCV000410562 RCV004529953 RCV001080937
ClinVar Variation Id: 1477741
ClinVar RCV Id: RCV001998437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1126Asp
CA288591
NM_032043.3:c.3378A>C
CA400478859
NM_032043.3:c.3378A>T