Canonical Allele Identifier: PA2580472172
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718808
ClinVar RCV Id: RCV002304913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1156Asp
CA400478664
NM_032043.3:c.3466A>G