Canonical Allele Identifier: PA645433504
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 231662
ClinVar RCV Id: RCV000219872 RCV000559529 RCV001533933 RCV003462473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn428Thr
CA8690768
NM_032043.3:c.1283A>C