Canonical Allele Identifier: PA2499292634
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043612
ClinVar RCV Id: RCV001347741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Cys1164Gly
CA400478559
NM_032043.3:c.3490T>G
CA2269130850
NM_032043.3:c.3489_3490delinsCG