Canonical Allele Identifier: PA1139759876
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 927484
ClinVar RCV Id: RCV001190794 RCV001863026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1063Pro
CA400479391
NM_032043.3:c.3187T>C