Canonical Allele Identifier: PA658663827
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 461151
ClinVar RCV Id: RCV000536947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1138His
CA400478785
NM_032043.3:c.3412G>C
CA658658649
NM_032043.3:c.3411_3412delinsCC