Canonical Allele Identifier: PA645436281
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 230724
ClinVar RCV Id: RCV000222116 RCV000521348 RCV000808973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1159Thr
CA10580771
NM_032043.3:c.3475G>A