Canonical Allele Identifier: PA2573287824
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1362150
ClinVar RCV Id: RCV001900035 RCV002458675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Tyr1131Cys
CA400478829
NM_032043.3:c.3392A>G