Canonical Allele Identifier: PA1139760013
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 853157
ClinVar RCV Id: RCV001057916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1095Pro
CA400479061
NM_032043.3:c.3283T>C