Canonical Allele Identifier: PA645436194
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro1092Ser
CA8690375
NM_032043.3:c.3274C>T