Canonical Allele Identifier: PA658724527
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 489833
ClinVar RCV Id: RCV000579866 RCV000636184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu1136Phe
CA400478797
NM_032043.3:c.3406C>T