Canonical Allele Identifier: PA1139760021
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 926653
ClinVar RCV Id: RCV001189347 RCV001587211 RCV001862993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1100His
CA400479033
NM_032043.3:c.3298G>C