Canonical Allele Identifier: PA645436205
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 233788
ClinVar RCV Id: RCV000217837 RCV003765440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu1093Phe
CA10580779
NM_032043.3:c.3277C>T