Canonical Allele Identifier: PA288587
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128185
ClinVar RCV Id: RCV000116154 RCV000204707 RCV000218787 RCV000663136 RCV000780057 RCV003315657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1079Thr
CA288585
NM_032043.3:c.3236T>C