Canonical Allele Identifier: PA2580472139
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2449928
ClinVar RCV Id: RCV003171869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1120Gly
CA400478902
NM_032043.3:c.3359A>G