Canonical Allele Identifier: PA658663821
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 461148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1130Val
CA400478837
NM_032043.3:c.3388A>G