Canonical Allele Identifier: PA645435485
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407876
ClinVar RCV Id: RCV000465302 RCV000589053 RCV000773139 RCV001563320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile902Thr
CA16615780
NM_032043.3:c.2705T>C