Canonical Allele Identifier: PA2741995166
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2953826
ClinVar RCV Id: RCV003813049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly768_Leu769del
CA2740093848
NM_032043.3:c.2303_2308del