Canonical Allele Identifier: PA1139760087
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 848802
ClinVar RCV Id: RCV001052634 RCV002451215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1130Met
CA400478834
NM_032043.3:c.3390C>G