Canonical Allele Identifier: PA916064538
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 643619
ClinVar RCV Id: RCV000797364 RCV001187109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1141Ala
CA292267261
NM_032043.3:c.3422A>C