Canonical Allele Identifier: PA191421
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 185240
ClinVar RCV Id: RCV000164623 RCV000551876 RCV003237749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1087Ser
CA191419
NM_032043.3:c.3260A>G