Canonical Allele Identifier: PA645436269
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374030
ClinVar RCV Id: RCV000414896 RCV000814484 RCV001199372 RCV003168605
ClinVar Variation Id: 3228127
ClinVar RCV Id: RCV004519837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1138Gly
CA16043535
NM_032043.3:c.3413A>G
CA2825002549
NM_032043.3:c.3411_3413delinsCGG