Canonical Allele Identifier: PA658724436
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 489831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.His1091Tyr
CA400479084
NM_032043.3:c.3271C>T