Allele Registry

Canonical Allele Identifier: PA645396398

Gene: C2CD3 HGNC NCBI

ClinVar RCV:

RCV000418985

ClinVar Variation:

389647

HGVS (amino-acid)	Matching Registered Transcripts
NP_056346.3:p.Asp1028Tyr	CA16606332 NM_015531.6:c.3082G>T