Canonical Allele Identifier: PA1139759977
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 919631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg1085Val
CA913187810
NM_032043.3:c.3253_3254delinsGT