Canonical Allele Identifier: PA2573287737
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1489068
ClinVar RCV Id: RCV001980439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.His1091Gln
CA400479080
NM_032043.3:c.3273T>G
CA400479081
NM_032043.3:c.3273T>A