Canonical Allele Identifier: PA165902
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 136149
ClinVar RCV Id: RCV000123358 RCV000442394 RCV000662393 RCV000130186 RCV001284121 RCV003315827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro1092Leu
CA165900
NM_032043.3:c.3275C>T