Canonical Allele Identifier: PA645436193
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1089Phe
CA8690377
NM_032043.3:c.3266C>T