Allele Registry

Canonical Allele Identifier: PA250662

Gene: DCC HGNC NCBI

ClinVar RCV:

RCV000018603

ClinVar Variation:

17074

HGVS (amino-acid)	Matching Registered Transcripts
NP_005206.2:p.Pro1375His	CA250661 NM_005215.4:c.4124C>A