Canonical Allele Identifier: PA165100
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141318
ClinVar RCV Id: RCV000129791 RCV000466396 RCV000424619 RCV003387768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg162Gln
CA165098
NM_032043.3:c.485G>A