Canonical Allele Identifier: PA2580472190
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2306679
ClinVar RCV Id: RCV004153281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1176Thr
CA400478409
NM_032043.3:c.3527T>C