Canonical Allele Identifier: PA157730
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128195
ClinVar RCV Id: RCV000116164 RCV000120409 RCV000411226 RCV000679792 RCV001082519 RCV001269494 RCV000409223 RCV000515771 RCV001798362 RCV004528813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg264Trp
CA157728
NM_032043.3:c.790C>T