Canonical Allele Identifier: PA288584
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 128184
ClinVar RCV Id: RCV000116153 RCV000212298 RCV000205068 RCV000409171 RCV000411175 RCV000780051 RCV004529952 RCV000990040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Arg106Cys
CA288582
NM_032043.3:c.316C>T