Canonical Allele Identifier: PA2580470657
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2014397
ClinVar RCV Id: RCV002830014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.His181Gln
CA400483209
NM_032043.3:c.543C>G
CA400483212
NM_032043.3:c.543C>A