Canonical Allele Identifier: PA2580470676
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1749924
ClinVar RCV Id: RCV002353191
ClinVar Variation Id: 1749935
ClinVar RCV Id: RCV002353202 RCV003096886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Lys194Asn
CA292277717
NM_032043.3:c.582A>T
CA400482996
NM_032043.3:c.582A>C