Canonical Allele Identifier: PA2499292728
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1201068
ClinVar RCV Id: RCV001566283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr609Pro
CA400480167
NM_032043.3:c.1825A>C