Canonical Allele Identifier: PA1139758767
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 848871
ClinVar RCV Id: RCV001052718 RCV002451216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile780Val
CA400482606
NM_032043.3:c.2338A>G