Canonical Allele Identifier: PA645432152
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 232285
ClinVar RCV Id: RCV000216902 RCV000467101 RCV003148687 RCV001354597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Met4Val
CA10580900
NM_032043.3:c.10A>G