Canonical Allele Identifier: PA193323
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 185905
ClinVar RCV Id: RCV000165410 RCV003765031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ile1130Phe
CA193321
NM_032043.3:c.3388A>T