Canonical Allele Identifier: PA2741995020
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2944360
ClinVar RCV Id: RCV003806110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly120Val
CA400485299
NM_032043.3:c.359G>T