Canonical Allele Identifier: PA2580470547
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733666
ClinVar RCV Id: RCV002452540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser122Leu
CA400485288
NM_032043.3:c.365C>T