Canonical Allele Identifier: PA645436210
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 230751
ClinVar RCV Id: RCV000220039 RCV000590421 RCV000701514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1097Ala
CA10580778
NM_032043.3:c.3290A>C