Canonical Allele Identifier: PA645436137
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407819
ClinVar RCV Id: RCV000457812 RCV000570958 RCV000662973 RCV003316562
ClinVar Variation Id: 1450375
ClinVar RCV Id: RCV002004830 RCV002442939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly1024Arg
CA8690405
NM_032043.3:c.3070G>A
CA400479875
NM_032043.3:c.3070G>C