Canonical Allele Identifier: PA190985
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 185090
ClinVar RCV Id: RCV000164450 RCV000409520 RCV000412033 RCV000520126 RCV000636160 RCV002247565 RCV003316022 RCV004528910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1032Arg
CA190983
NM_032043.3:c.3096T>G
CA400479766
NM_032043.3:c.3096T>A
CA400479778
NM_032043.3:c.3094A>C