Canonical Allele Identifier: PA157694
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133752
ClinVar RCV Id: RCV000120396 RCV000123354 RCV000131414 RCV000488342 RCV000411134 RCV000778128 RCV000989999 RCV000409608 RCV001358098 RCV001798382 RCV003492522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Gln740His
CA157692
NM_032043.3:c.2220G>T
CA8690571
NM_032043.3:c.2220G>C