Allele Registry

Canonical Allele Identifier: PA915997369

Gene: CTCF HGNC NCBI

ClinVar RCV:

RCV000255519

ClinVar Variation:

265526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177951.1:p.Tyr79Cys	CA10588621 NM_001191022.2:c.236A>G