Canonical Allele Identifier: PA916064568
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1156Ser
CA400478660
NM_032043.3:c.3467A>G