Canonical Allele Identifier: PA163755
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 140858
ClinVar RCV Id: RCV000129066 RCV001561211 RCV003460885 RCV000470192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Tyr369His
CA163753
NM_032043.3:c.1105T>C