Canonical Allele Identifier: PA658663668
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 483140
ClinVar RCV Id: RCV000565343 RCV001300400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser876Asn
CA8690468
NM_032043.3:c.2627G>A