Canonical Allele Identifier: PA288534
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128162
ClinVar RCV Id: RCV000116130 RCV000196018 RCV000412043 RCV000212315 RCV000410174 RCV001192970 RCV003315649 RCV004528811
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg579Cys
CA288532
NM_032043.3:c.1735C>T