Canonical Allele Identifier: PA658665630
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 461122
ClinVar RCV Id: RCV000558834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala89Thr
CA400485501
NM_032043.3:c.265G>A