Canonical Allele Identifier: PA1139760051
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 952055
ClinVar RCV Id: RCV001224097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1110Lys
CA400478971
NM_032043.3:c.3328G>A