Canonical Allele Identifier: PA2580472080
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729545
ClinVar RCV Id: RCV002324976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.His1088Asp
CA400479103
NM_032043.3:c.3262C>G