Canonical Allele Identifier: PA658663786
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 461143
ClinVar RCV Id: RCV000540633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.His1091Arg
CA8690376
NM_032043.3:c.3272A>G