Canonical Allele Identifier: PA1139760070
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 958513
ClinVar RCV Id: RCV001231696 RCV001523996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn1118Asp
CA400478919
NM_032043.3:c.3352A>G