Canonical Allele Identifier: PA2580472073
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729441
ClinVar RCV Id: RCV002324905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg1085Gly
CA400479126
NM_032043.3:c.3253A>G