Canonical Allele Identifier: PA2499292746
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046186
ClinVar RCV Id: RCV001350707 RCV003294378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1066Pro
CA400479359
NM_032043.3:c.3196T>C