Canonical Allele Identifier: PA2573287718
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372935
ClinVar RCV Id: RCV001874941 RCV003585001 RCV003442937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1080Tyr
CA400479180
NM_032043.3:c.3238G>T