Canonical Allele Identifier: PA168726
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu1170Val
CA168724
NM_032043.3:c.3508C>G