Allele Registry

Canonical Allele Identifier: PA163766

Gene: BRIP1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

150575

950096

ClinVar RCV:

RCV000129073

RCV000636097

RCV001233351

RCV003166432

RCV003321509

ClinVar Variation:

140861

959917

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Gly1009Arg	CA163764 NM_032043.3:c.3025G>A CA400479967 NM_032043.3:c.3025G>C