Canonical Allele Identifier: PA658663797
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 479410
ClinVar RCV Id: RCV000565197 RCV000636089 RCV003228956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1112Tyr
CA292267318
NM_032043.3:c.3334G>T