Canonical Allele Identifier: PA916064632
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 641679
ClinVar RCV Id: RCV000794973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Glu1178Gln
CA400478386
NM_032043.3:c.3532G>C