Canonical Allele Identifier: PA645436179
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 233975
ClinVar RCV Id: RCV000215579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1084Ile
CA10580781
NM_032043.3:c.3251C>T