Canonical Allele Identifier: PA2580472160
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1731229
ClinVar RCV Id: RCV002452209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1140Lys
CA400478774
NM_032043.3:c.3418G>A