Canonical Allele Identifier: PA645436236
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1112Asn
CA16615474
NM_032043.3:c.3334G>A