Canonical Allele Identifier: PA658663392
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 483156
ClinVar RCV Id: RCV000563546 RCV001372997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asn471Ser
CA400482165
NM_032043.3:c.1412A>G