Canonical Allele Identifier: PA1139760194
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 949635
ClinVar RCV Id: RCV001221135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1135Gly
CA400478803
NM_032043.3:c.3404A>G