Allele Registry

Canonical Allele Identifier: PA110396

Gene: CTCF HGNC NCBI

ClinVar RCV:

RCV000074335

RCV000413282

RCV002260512

RCV002399425

ClinVar Variation:

88638

HGVS (amino-acid)	Matching Registered Transcripts
NP_006556.1:p.Arg567Trp	CA10575614 NM_006565.4:c.1699C>T