Allele Registry

Canonical Allele Identifier: PA117564

Gene: TRIP11 HGNC NCBI

ClinVar RCV:

RCV000005846

RCV000725982

RCV002276533

ClinVar Variation:

5511

HGVS (amino-acid)	Matching Registered Transcripts
NP_004230.2:p.Asn701Ser	CA117563 NM_004239.4:c.2102A>G