Canonical Allele Identifier: PA645436080
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 232950
ClinVar RCV Id: RCV000214349 RCV000215700 RCV000227974 RCV000709536 RCV000989990 RCV001194733 RCV000662447 RCV001030466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile952Val
CA8690447
NM_032043.3:c.2854A>G