Canonical Allele Identifier: PA645436271
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 232616
ClinVar RCV Id: RCV000459206 RCV000223506 RCV000587926 RCV000709525
ClinVar Variation Id: 491468
ClinVar RCV Id: RCV000583646 RCV000586252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1138Asn
CA8690365
NM_032043.3:c.3412G>A
CA658684147
NM_032043.3:c.3411_3412delinsCA