Canonical Allele Identifier: PA2499292699
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 999596
ClinVar RCV Id: RCV001295613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1176Val
CA400478414
NM_032043.3:c.3526A>G