Canonical Allele Identifier: PA168133
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142346
ClinVar RCV Id: RCV000131421 RCV000234751 RCV000410875 RCV000409672 RCV000759709 RCV000989996 RCV003479018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile782Val
CA168131
NM_032043.3:c.2344A>G