Canonical Allele Identifier: PA2830079556
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3228128
ClinVar RCV Id: RCV004519838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala1150Asp
CA400478702
NM_032043.3:c.3449C>A