Canonical Allele Identifier: PA913199231
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 631323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1087Lys
CA400479105
NM_032043.3:c.3261T>G
CA400479106
NM_032043.3:c.3261T>A