Canonical Allele Identifier: PA298886
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 182350
ClinVar RCV Id: RCV000160340 RCV000532063 RCV000581551 RCV002466455
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly120Asp
CA298884
NM_032043.3:c.359G>A