Canonical Allele Identifier: PA165063
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141305
ClinVar RCV Id: RCV000129774 RCV000478765 RCV001088100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys897Glu
CA165061
NM_032043.3:c.2689A>G