Canonical Allele Identifier: PA356928
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 219832
ClinVar RCV Id: RCV000206799 RCV000409113 RCV000411587 RCV000581063 RCV002466467 RCV003316132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1144Gly
CA350798
NM_032043.3:c.3431A>G