Canonical Allele Identifier: PA891851832
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 575616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg1085Thr
CA400479123
NM_032043.3:c.3254G>C