Canonical Allele Identifier: PA658816865
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530325
ClinVar RCV Id: RCV000636129 RCV000775419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg579His
CA8690680
NM_032043.3:c.1736G>A