Canonical Allele Identifier: PA916064565
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 803447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg1154Gly
CA8690362
NM_032043.3:c.3460A>G