Canonical Allele Identifier: PA157737
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30535
ClinVar RCV Id: RCV000023492 RCV000120412 RCV000131544 RCV000216316 RCV000466014 RCV000761010 RCV002271374 RCV003335053 RCV004528133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114432.2:p.Ala349Pro
CA157735
NM_032043.3:c.1045G>C