Canonical Allele Identifier: PA157712
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133758
ClinVar RCV Id: RCV000120402 RCV000131003 RCV000204453 RCV000409042 RCV000411479 RCV000589005 RCV000989978 RCV001535623 RCV003149828
ClinVar Variation Id: 823778
ClinVar RCV Id: RCV001020320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Asp1148Glu
CA157710
NM_032043.3:c.3444C>A
CA400478710
NM_032043.3:c.3444C>G