Canonical Allele Identifier: PA916064589
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1159Pro
CA400478625
NM_032043.3:c.3475G>C