Canonical Allele Identifier: PA916064666
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 824006
ClinVar RCV Id: RCV001020751 RCV001860998 RCV004545017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1209Val
CA400477978
NM_032043.3:c.3625A>G