Canonical Allele Identifier: PA658817180
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530309
ClinVar RCV Id: RCV000636098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1120Asn
CA400478905
NM_032043.3:c.3358G>A