Canonical Allele Identifier: PA2580471181
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1781689
ClinVar RCV Id: RCV002415106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser624Pro
CA400480071
NM_032043.3:c.1870T>C