Canonical Allele Identifier: PA1139760255
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 929141
ClinVar RCV Id: RCV001194198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1142Ala
CA400478758
NM_032043.3:c.3424A>G