Canonical Allele Identifier: PA2499292718
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001509
ClinVar RCV Id: RCV001297819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Tyr369Ser
CA400483920
NM_032043.3:c.1106A>C