Canonical Allele Identifier: PA2580472125
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721734
ClinVar RCV Id: RCV002294982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys1113Gln
CA400478953
NM_032043.3:c.3337A>C