Canonical Allele Identifier: PA645433654
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 232167
ClinVar RCV Id: RCV000218250 RCV000227822 RCV002222450 RCV002291600 RCV003238743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp563Gly
CA8690687
NM_032043.3:c.1688A>G