Canonical Allele Identifier: PA2573287907
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1496891
ClinVar RCV Id: RCV001992111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg1174Gly
CA400478436
NM_032043.3:c.3520A>G