Canonical Allele Identifier: PA645433766
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421095
ClinVar RCV Id: RCV000478238 RCV000818704 RCV002413328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly628Val
CA16620526
NM_032043.3:c.1883G>T