Canonical Allele Identifier: PA195887
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186793
ClinVar RCV Id: RCV000166442 RCV000472014 RCV000662959 RCV000989986 RCV002259316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Val972Ile
CA195885
NM_032043.3:c.2914G>A