Canonical Allele Identifier: PA658663661
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 461119
ClinVar RCV Id: RCV000546088 RCV000575702 RCV000679781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Val864Ile
CA8690474
NM_032043.3:c.2590G>A