Canonical Allele Identifier: PA166083
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141666
ClinVar RCV Id: RCV000130274 RCV000546539 RCV001284122 RCV000989980 RCV002267875
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1100Asn
CA166081
NM_032043.3:c.3298G>A