Canonical Allele Identifier: PA2580470693
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1751680
ClinVar RCV Id: RCV002360228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser204Pro
CA400482853
NM_032043.3:c.610T>C