Canonical Allele Identifier: PA913199242
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 628185
ClinVar RCV Id: RCV000772523 RCV001219320 RCV003461026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1104Val
CA400479005
NM_032043.3:c.3311A>T