Canonical Allele Identifier: PA2580471958
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2090575
ClinVar RCV Id: RCV003013172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1016Met
CA400479916
NM_032043.3:c.3048A>G