Canonical Allele Identifier: PA2741995233
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2950154
ClinVar RCV Id: RCV003807512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg1119Thr
CA400478910
NM_032043.3:c.3356G>C