Canonical Allele Identifier: PA190620
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 184968
ClinVar RCV Id: RCV000164317 RCV000234088 RCV000662914 RCV001194773 RCV001706079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp753Gly
CA190618
NM_032043.3:c.2258A>G