Canonical Allele Identifier: PA192864
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 185764
ClinVar RCV Id: RCV000165248 RCV000460048 RCV002307422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr124Pro
CA192862
NM_032043.3:c.370A>C