Canonical Allele Identifier: PA165400
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly1024Val
CA165398
NM_032043.3:c.3071G>T