Canonical Allele Identifier: PA645436245
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 419472
ClinVar RCV Id: RCV000484914 RCV000701214 RCV000570953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1124Gly
CA16620510
NM_032043.3:c.3371A>G