Canonical Allele Identifier: PA2573096664
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1321103
ClinVar RCV Id: RCV001777082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro1134Ser
CA292267279
NM_032043.3:c.3400C>T