Canonical Allele Identifier: PA1139757336
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 962804
ClinVar RCV Id: RCV001236726 RCV002379904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys433Glu
CA400483494
NM_032043.3:c.1297A>G