Canonical Allele Identifier: PA2741995236
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2774980
ClinVar RCV Id: RCV003585038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Phe1132Leu
CA400478818
NM_032043.3:c.3396T>G
CA400478819
NM_032043.3:c.3396T>A
CA400478824
NM_032043.3:c.3394T>C