Canonical Allele Identifier: PA2580472216
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732967
ClinVar RCV Id: RCV002455123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly1197Arg
CA400478133
NM_032043.3:c.3589G>A
CA400478135
NM_032043.3:c.3589G>C