Canonical Allele Identifier: PA2573287696
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1446636
ClinVar RCV Id: RCV001987760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Cys1067Phe
CA400479338
NM_032043.3:c.3200G>T