Canonical Allele Identifier: PA658663858
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 483173
ClinVar RCV Id: RCV000569978 RCV000989970 RCV001055410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1231Met
CA292267084
NM_032043.3:c.3693A>G