Canonical Allele Identifier: PA916064479
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 661153
ClinVar RCV Id: RCV000818513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1128Lys
CA292267292
NM_032043.3:c.3382G>A