Canonical Allele Identifier: PA2741995229
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2774982
ClinVar RCV Id: RCV003585040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1098Thr
CA400479043
NM_032043.3:c.3292G>A