Canonical Allele Identifier: PA168411
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142458
ClinVar RCV Id: RCV000131589 RCV000220020 RCV000588637 RCV000663050 RCV001082225 RCV002225445 RCV003315912 RCV003492626 RCV004532572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg106His
CA168409
NM_032043.3:c.317G>A