Canonical Allele Identifier: PA189778
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 184706
ClinVar RCV Id: RCV000164008 RCV000197368 RCV000662667 RCV001797647 RCV003316014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile962Thr
CA189776
NM_032043.3:c.2885T>C