Canonical Allele Identifier: PA2741995235
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2692012
ClinVar RCV Id: RCV003494209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1129Phe
CA400478839
NM_032043.3:c.3386C>T