Canonical Allele Identifier: PA165878
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141590
ClinVar RCV Id: RCV000130174 RCV000484934 RCV000709557 RCV000473070 RCV000990023 RCV003321513 RCV003492596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile243Thr
CA165876
NM_032043.3:c.728T>C