Canonical Allele Identifier: PA2580470851
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796849
ClinVar RCV Id: RCV002435380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Leu373Pro
CA400483895
NM_032043.3:c.1118T>C