Canonical Allele Identifier: PA2741995237
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2922129
ClinVar RCV Id: RCV003785343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1144Gln
CA400478744
NM_032043.3:c.3430G>C