Canonical Allele Identifier: PA1139760390
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 954168
ClinVar RCV Id: RCV001226578
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1173Leu
CA400478446
NM_032043.3:c.3517A>C