Canonical Allele Identifier: PA165146
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141336
ClinVar RCV Id: RCV000129821 RCV000200144 RCV000662741 RCV000758998 RCV000780068 RCV003315884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1079Met
CA165144
NM_032043.3:c.3237T>G