Canonical Allele Identifier: PA151534
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128198
ClinVar RCV Id: RCV000116167 RCV000120408 RCV000410013 RCV000412293 RCV000590718 RCV000990022 RCV001084039 RCV001354244 RCV001798363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys297Arg
CA151532
NM_032043.3:c.890A>G