Canonical Allele Identifier: PA2573293097
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1414257
ClinVar RCV Id: RCV001928600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr121Ile
CA400485294
NM_032043.3:c.362C>T