Canonical Allele Identifier: PA891851489
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 570984
ClinVar RCV Id: RCV000691993 RCV001183078
ClinVar Variation Id: 645839
ClinVar RCV Id: RCV000800003
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser444Arg
CA400483328
NM_032043.3:c.1332C>G
CA400483331
NM_032043.3:c.1332C>A
CA400483346
NM_032043.3:c.1330A>C