Canonical Allele Identifier: PA294432
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142529
ClinVar RCV Id: RCV000131711 RCV000212326 RCV001220332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg848Ser
CA294430
NM_032043.3:c.2542C>A