Canonical Allele Identifier: PA2499292633
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043014
ClinVar RCV Id: RCV001347059
ClinVar Variation Id: 1731326
ClinVar RCV Id: RCV002456995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1143Glu
CA400478746
NM_032043.3:c.3429T>A
CA400478747
NM_032043.3:c.3429T>G