Canonical Allele Identifier: PA2580472017
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728345
ClinVar RCV Id: RCV002322548 RCV003775060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1055Tyr
CA400479477
NM_032043.3:c.3164C>A