Canonical Allele Identifier: PA645509962
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 439028
ClinVar RCV Id: RCV000506530 RCV000701820 RCV002455976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys1168Thr
CA8690355
NM_032043.3:c.3503A>C