Canonical Allele Identifier: PA645436265
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 386141
ClinVar RCV Id: RCV000441972 RCV000775924 RCV000820751 RCV003444232 RCV004539857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1130Thr
CA16607741
NM_032043.3:c.3389T>C