Allele Registry

Canonical Allele Identifier: PA2826170435

Gene: CTCF HGNC NCBI

ClinVar RCV:

RCV000074335

RCV000413282

RCV002260512

RCV002399425

ClinVar Variation:

88638

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177951.1:p.Arg239Trp	CA10575614 NM_001191022.2:c.715C>T