Canonical Allele Identifier: PA2573287874
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1510643
ClinVar RCV Id: RCV002014020 RCV002460180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu1158Met
CA400478636
NM_032043.3:c.3472T>A