Canonical Allele Identifier: PA658831678
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 560879
ClinVar RCV Id: RCV000679787 RCV001228582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Phe1248Leu
CA400477700
NM_032043.3:c.3744T>G
CA400477701
NM_032043.3:c.3744T>A
CA400477705
NM_032043.3:c.3742T>C