Canonical Allele Identifier: PA2573287690
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516421
ClinVar RCV Id: RCV002026581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Phe1064Leu
CA400479369
NM_032043.3:c.3192T>G
CA400479371
NM_032043.3:c.3192T>A
CA400479379
NM_032043.3:c.3190T>C