Canonical Allele Identifier: PA913198811
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 631313
ClinVar RCV Id: RCV000777494 RCV000797303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr121Ala
CA400485298
NM_032043.3:c.361A>G