Canonical Allele Identifier: PA2580472140
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2059395
ClinVar RCV Id: RCV002933707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1120His
CA400478906
NM_032043.3:c.3358G>C