Canonical Allele Identifier: PA645436335
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 232920
ClinVar RCV Id: RCV000222505 RCV000636105 RCV001262871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro1246Leu
CA10580767
NM_032043.3:c.3737C>T