Canonical Allele Identifier: PA658817222
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 506573
ClinVar RCV Id: RCV000606452 RCV001860262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ser1237Tyr
CA400477772
NM_032043.3:c.3710C>A