Canonical Allele Identifier: PA916062300
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 818411
ClinVar RCV Id: RCV001009975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu379Lys
CA400483862
NM_032043.3:c.1135G>A