Canonical Allele Identifier: PA165330
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141402
ClinVar RCV Id: RCV000129907 RCV000227303 RCV000657056 RCV000989972 RCV003492594
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Trp1217Cys
CA165328
NM_032043.3:c.3651G>T
CA400477901
NM_032043.3:c.3651G>C