Canonical Allele Identifier: PA645436313
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 419945
ClinVar RCV Id: RCV000482446 RCV000802727 RCV001020755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1210del
CA16620506
NM_032043.3:c.3629_3631del