Canonical Allele Identifier: PA1139760027
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 954593
ClinVar RCV Id: RCV001227079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1100Tyr
CA400479034
NM_032043.3:c.3298G>T