Canonical Allele Identifier: PA2499292670
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062356
ClinVar RCV Id: RCV001372059 RCV002432048
ClinVar Variation Id: 2942807
ClinVar RCV Id: RCV003807973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Phe771Leu
CA400482654
NM_032043.3:c.2313C>G
CA400482655
NM_032043.3:c.2313C>A
CA400482660
NM_032043.3:c.2311T>C