Canonical Allele Identifier: PA1139760079
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 920489
ClinVar RCV Id: RCV001179247 RCV001222155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1128Gln
CA400478850
NM_032043.3:c.3382G>C