Canonical Allele Identifier: PA1139757241
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 962515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Phe417Leu
CA400483600
NM_032043.3:c.1251T>G
CA400483601
NM_032043.3:c.1251T>A
CA400483606
NM_032043.3:c.1249T>C