Canonical Allele Identifier: PA356766
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 220245
ClinVar RCV Id: RCV000216628 RCV000255184 RCV000205088
ClinVar Variation Id: 965739
ClinVar RCV Id: RCV001240256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1169Glu
CA349272
NM_032043.3:c.3507C>A
CA400478491
NM_032043.3:c.3507C>G