Canonical Allele Identifier: PA658724422
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 496484
ClinVar RCV Id: RCV000589375 RCV003302906 RCV003767343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1081Val
CA400479154
NM_032043.3:c.3242C>T