Canonical Allele Identifier: PA194300
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186266
ClinVar RCV Id: RCV000165832 RCV000477468 RCV000506104 RCV001357851 RCV004539555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu1099Arg
CA194298
NM_032043.3:c.3296T>G