Canonical Allele Identifier: PA163669
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 140825
ClinVar RCV Id: RCV000129015 RCV000197620 RCV000213740 RCV000662424 RCV003315868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1050Asn
CA163667
NM_032043.3:c.3149C>A