Canonical Allele Identifier: PA339378
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 216790
ClinVar RCV Id: RCV000200543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Cys87Tyr
CA339376
NM_032043.3:c.260G>A