Canonical Allele Identifier: PA2580471188
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1782177
ClinVar RCV Id: RCV002408132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile633Val
CA8690638
NM_032043.3:c.1897A>G