Canonical Allele Identifier: PA658663824
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 461150
ClinVar RCV Id: RCV000560658 RCV001020189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Thr1133Ile
CA400478812
NM_032043.3:c.3398C>T