Canonical Allele Identifier: PA2580472189
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1176Met
CA400478405
NM_032043.3:c.3528A>G