Canonical Allele Identifier: PA1139759891
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 925380
ClinVar RCV Id: RCV001187262 RCV001219207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1066Thr
CA400479360
NM_032043.3:c.3196T>A