Canonical Allele Identifier: PA2741995129
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626397
ClinVar RCV Id: RCV003382377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala599Asp
CA400480231
NM_032043.3:c.1796C>A