Canonical Allele Identifier: PA2741995145
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2953041
ClinVar RCV Id: RCV003810159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly657Ser
CA400478529
NM_032043.3:c.1969G>A