Canonical Allele Identifier: PA916064322
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 653008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu1093Val
CA400479075
NM_032043.3:c.3277C>G