Canonical Allele Identifier: PA658665844
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 461060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu372Phe
CA292286069
NM_032043.3:c.1114C>T