Canonical Allele Identifier: PA2499292631
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1098Asp
CA400479041
NM_032043.3:c.3293C>A