Canonical Allele Identifier: PA208857
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128169
ClinVar RCV Id: RCV000116137 RCV000194594 RCV000477497 RCV000586157 RCV000662754 RCV001762241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala745Thr
CA208855
NM_032043.3:c.2233G>A