Canonical Allele Identifier: PA2580472112
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730146
ClinVar RCV Id: RCV002454732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1106Cys
CA400478992
NM_032043.3:c.3317C>G