Allele Registry

Canonical Allele Identifier: PA2828128226

Gene: CTCF HGNC NCBI

ClinVar RCV:

RCV000255519

ClinVar Variation:

265526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350845.1:p.Tyr407Cys	CA10588621 NM_001363916.1:c.1220A>G