Canonical Allele Identifier: PA1139760230
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 858986
ClinVar RCV Id: RCV001064987 RCV001357702
ClinVar Variation Id: 1049276
ClinVar RCV Id: RCV001355199 RCV002456533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Tyr1137His
CA400478793
NM_032043.3:c.3409T>C
CA2499224774
NM_032043.3:c.3409_3411delinsCAC