Canonical Allele Identifier: PA658816806
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530288
ClinVar RCV Id: RCV000636064 RCV001011049 RCV003441985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Cys443Tyr
CA400483360
NM_032043.3:c.1328G>A