Canonical Allele Identifier: PA164121
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 140985
ClinVar RCV Id: RCV000129283 RCV000409964 RCV000412403 RCV000636117 RCV001775619 RCV003315873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile983Asn
CA164119
NM_032043.3:c.2948T>A