Canonical Allele Identifier: PA190068
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 184796
ClinVar RCV Id: RCV000164112 RCV000475560 RCV001356649 RCV000439785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Val518Ile
CA190066
NM_032043.3:c.1552G>A