Canonical Allele Identifier: PA891851842
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 568102
ClinVar RCV Id: RCV000688353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1115Pro
CA400478936
NM_032043.3:c.3343T>C