Canonical Allele Identifier: PA2580472122
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730253
ClinVar RCV Id: RCV002326429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1109Ile
CA400478976
NM_032043.3:c.3326G>T