Canonical Allele Identifier: PA294224
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141975
ClinVar RCV Id: RCV000130729 RCV000212311 RCV000469846 RCV000663131 RCV000780054 RCV001030540 RCV001124864 RCV003315897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gly481Asp
CA294222
NM_032043.3:c.1442G>A