Canonical Allele Identifier: PA2499292698
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024791
ClinVar RCV Id: RCV001325016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu1166Ser
CA400478532
NM_032043.3:c.3497T>C