Canonical Allele Identifier: PA334787
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 188402
ClinVar RCV Id: RCV000168472 RCV000485677 RCV001020125 RCV001355547 RCV003321537 RCV003491923 RCV003483553
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1125del
CA334785
NM_032043.3:c.3374_3376del