Canonical Allele Identifier: PA658816620
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530299
ClinVar RCV Id: RCV000636078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Cys88Gly
CA400485507
NM_032043.3:c.262T>G