Canonical Allele Identifier: PA2741995231
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564610
ClinVar RCV Id: RCV003297042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1106Phe
CA400478991
NM_032043.3:c.3317C>T