Canonical Allele Identifier: PA2499292673
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057933
ClinVar RCV Id: RCV001367007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly830Ser
CA400479395
NM_032043.3:c.2488G>A