Canonical Allele Identifier: PA2573287798
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1470182
ClinVar RCV Id: RCV001995149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1122Gly
CA400478886
NM_032043.3:c.3365A>G