Canonical Allele Identifier: PA658724442
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 491464
ClinVar RCV Id: RCV000581888 RCV000636141 RCV000989981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Pro1092Gln
CA400479077
NM_032043.3:c.3275C>A