Allele Registry

Canonical Allele Identifier: PA092997

Gene: CTC1 HGNC NCBI

ClinVar RCV:

RCV000023993

RCV003227608

ClinVar Variation:

31002

HGVS (amino-acid)	Matching Registered Transcripts
NP_079375.3:p.Val665Gly	CA129614 NM_025099.6:c.1994T>G