Canonical Allele Identifier: PA194106
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186189
ClinVar RCV Id: RCV000165735 RCV000410856 RCV000412383 RCV000542964 RCV001778762 RCV001847787 RCV003316047
ClinVar Variation Id: 241635
ClinVar RCV Id: RCV000226066 RCV000481541 RCV000582028 RCV000709542 RCV000990006 RCV003482141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Trp647Cys
CA194104
NM_032043.3:c.1941G>T
CA10583627
NM_032043.3:c.1941G>C