Canonical Allele Identifier: PA1139760009
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 871754
ClinVar RCV Id: RCV001091878 RCV002445379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1095Cys
CA400479059
NM_032043.3:c.3284C>G