Canonical Allele Identifier: PA1139760229
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 936091
ClinVar RCV Id: RCV001204817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu1136Arg
CA400478794
NM_032043.3:c.3407T>G