Canonical Allele Identifier: PA334049
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 188103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1072Asn
CA334047
NM_032043.3:c.3215C>A