Canonical Allele Identifier: PA157718
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133760
ClinVar RCV Id: RCV000120404 RCV000131536 RCV000589730 RCV001355323 RCV000408974 RCV000410510 RCV003315738 RCV001084094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala144Thr
CA157716
NM_032043.3:c.430G>A