Allele Registry

Canonical Allele Identifier: PA645503444

Gene: CTCF HGNC NCBI

ClinVar RCV:

RCV000255519

ClinVar Variation:

265526

HGVS (amino-acid)	Matching Registered Transcripts
NP_006556.1:p.Tyr407Cys	CA10588621 NM_006565.4:c.1220A>G