Canonical Allele Identifier: PA645433303
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407853
ClinVar RCV Id: RCV000473551 RCV001525372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Tyr371Cys
CA16615528
NM_032043.3:c.1112A>G