Canonical Allele Identifier: PA2741995228
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2921774
ClinVar RCV Id: RCV003782796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys1086Glu
CA400479118
NM_032043.3:c.3256A>G