Canonical Allele Identifier: PA2573287743
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442619
ClinVar RCV Id: RCV001953086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro1092Arg
CA400479076
NM_032043.3:c.3275C>G