Canonical Allele Identifier: PA163645
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 140819
ClinVar RCV Id: RCV000129008 RCV000410906 RCV000412441 RCV000590794 RCV001081667 RCV001800423 RCV003149886 RCV001355322 RCV004532542 RCV003315867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg1035Cys
CA163643
NM_032043.3:c.3103C>T