Canonical Allele Identifier: PA645432840
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407803
ClinVar RCV Id: RCV000458246 RCV001185470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly190Glu
CA8690908
NM_032043.3:c.569G>A