Canonical Allele Identifier: PA1139758083
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 920730
ClinVar RCV Id: RCV001179676 RCV001875945
ClinVar Variation Id: 946555
ClinVar RCV Id: RCV001217442 RCV002411805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu626Asp
CA400480043
NM_032043.3:c.1878A>T
CA400480044
NM_032043.3:c.1878A>C