Canonical Allele Identifier: PA891851840
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 577717
ClinVar RCV Id: RCV000700540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Val1108Ile
CA400478985
NM_032043.3:c.3322G>A