Canonical Allele Identifier: PA2580472128
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719279
ClinVar RCV Id: RCV002302039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gln1114Pro
CA400478942
NM_032043.3:c.3341A>C