Canonical Allele Identifier: PA2580471183
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714137
ClinVar RCV Id: RCV002297120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser625Leu
CA400480057
NM_032043.3:c.1874C>T