Canonical Allele Identifier: PA645432974
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 419001
ClinVar RCV Id: RCV000484748 RCV000823332 RCV000775425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly290Ser
CA8690840
NM_032043.3:c.868G>A