Canonical Allele Identifier: PA298874
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 182346
ClinVar RCV Id: RCV000160336 RCV000565573 RCV001300398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile359Met
CA298872
NM_032043.3:c.1077A>G