Canonical Allele Identifier: PA294542
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 143021
ClinVar RCV Id: RCV000132540 RCV000168177 RCV000212302 RCV000662870 RCV001192824 RCV001196849 RCV001358268 RCV003315923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp184Tyr
CA294540
NM_032043.3:c.550G>T